ENST00000350026.11:c.3867T>C
|
ENSP00000055163.8:p.Pro1289=
|
|
ENST00000414678.8:c.3936T>C
|
ENSP00000412835.3:p.Pro1312=
|
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ENST00000637015.2:c.4155T>C
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ENSP00000489729.2:p.Pro1385=
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ENST00000346085.10:c.3906T>C
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ENSP00000344546.5:p.Pro1302=
|
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ENST00000350026.10:c.3618T>C
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ENSP00000055163.7:p.Pro1206=
|
|
ENST00000414678.7:c.2184T>C
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ENSP00000412835.2:p.Pro728=
|
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ENST00000635849.1:c.1347T>C
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ENSP00000490948.1:p.Pro449=
|
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ENST00000635957.1:c.981T>C
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ENSP00000490385.1:p.Pro327=
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ENST00000636930.2:c.4026T>C
MANE Select
|
ENSP00000490491.2:p.Pro1342=
|
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ENST00000636940.1:n.2023T>C
|
|
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ENST00000637015.1:c.1394T>C
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ENST00000637568.1:c.1308T>C
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|
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ENST00000637741.1:n.692T>C
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ENST00000637810.1:c.1368T>C
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ENSP00000489636.1:p.Pro456=
|
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ENST00000637904.1:c.1527T>C
|
ENSP00000490550.1:p.Pro509=
|
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ENST00000647938.1:c.3657T>C
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ENSP00000498155.1:p.Pro1219=
|
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ENST00000346085.9:c.3657T>C
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ENSP00000344546.4:p.Pro1219=
|
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ENST00000350026.9:c.3618T>C
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ENSP00000055163.7:p.Pro1206=
|
|
ENST00000414678.6:c.2184T>C
|
ENSP00000412835.2:p.Pro728=
|
|
NM_017519.2:c.3618T>C
|
NP_059989.2:p.Pro1206=
|
|
NM_020732.3:c.3657T>C
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NP_065783.3:p.Pro1219=
|
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XM_005267069.3:c.3777T>C
|
XP_005267126.2:p.Pro1259=
|
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XM_011535984.1:c.2856T>C
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XP_011534286.1:p.Pro952=
|
|
XM_011535985.1:c.2676T>C
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XP_011534287.1:p.Pro892=
|
|
XM_011535986.1:c.2436T>C
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XP_011534288.1:p.Pro812=
|
|
XM_011535987.1:c.2055T>C
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XP_011534289.1:p.Pro685=
|
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XM_011535988.1:c.918T>C
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XP_011534290.1:p.Pro306=
|
|
NM_001346813.1:c.3777T>C
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NP_001333742.1:p.Pro1259=
|
|
NM_001363725.1:c.1527T>C
|
NP_001350654.1:p.Pro509=
|
|
XM_011535984.2:c.3987T>C
|
XP_011534286.2:p.Pro1329=
|
|
XM_011535988.3:c.918T>C
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XP_011534290.1:p.Pro306=
|
|
XM_017011103.2:c.3888T>C
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XP_016866592.1:p.Pro1296=
|
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XM_017011104.1:c.3858T>C
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XP_016866593.1:p.Pro1286=
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XM_017011105.2:c.3828T>C
|
XP_016866594.1:p.Pro1276=
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XM_017011106.2:c.3699T>C
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XP_016866595.1:p.Pro1233=
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XM_017011107.2:c.3678T>C
|
XP_016866596.1:p.Pro1226=
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XR_002956289.1:n.4070T>C
|
|
|
NM_001363725.2:c.1527T>C
|
NP_001350654.1:p.Pro509=
|
|
NM_001371656.1:c.3906T>C
|
NP_001358585.1:p.Pro1302=
|
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NM_001374820.1:c.3906T>C
|
NP_001361749.1:p.Pro1302=
|
|
NM_001374828.1:c.4026T>C
MANE Select
|
NP_001361757.1:p.Pro1342=
|
|
NM_017519.3:c.3867T>C
|
NP_059989.3:p.Pro1289=
|
|