ENST00000350026.11:c.3018A>C
|
ENSP00000055163.8:p.Pro1006=
|
|
ENST00000414678.8:c.2928A>C
|
ENSP00000412835.3:p.Pro976=
|
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ENST00000637015.2:c.3018A>C
|
ENSP00000489729.2:p.Pro1006=
|
|
ENST00000319584.11:c.1032A>C
|
ENSP00000313006.7:p.Pro344=
|
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ENST00000346085.10:c.3057A>C
|
ENSP00000344546.5:p.Pro1019=
|
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ENST00000350026.10:c.2769A>C
|
ENSP00000055163.7:p.Pro923=
|
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ENST00000414678.7:c.1176A>C
|
ENSP00000412835.2:p.Pro392=
|
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ENST00000452544.2:n.919A>C
|
|
|
ENST00000635849.1:c.339A>C
|
ENSP00000490948.1:p.Pro113=
|
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ENST00000636426.1:n.152A>C
|
|
|
ENST00000636930.2:c.3018A>C
MANE Select
|
ENSP00000490491.2:p.Pro1006=
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ENST00000637015.1:c.257A>C
|
|
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ENST00000637568.1:c.61A>C
|
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ENST00000637810.1:c.519A>C
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ENSP00000489636.1:p.Pro173=
|
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ENST00000637904.1:c.519A>C
|
ENSP00000490550.1:p.Pro173=
|
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ENST00000647938.1:c.2808A>C
|
ENSP00000498155.1:p.Pro936=
|
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ENST00000674190.1:n.1767A>C
|
|
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ENST00000319584.10:c.1035A>C
|
ENSP00000313006.6:p.Pro345=
|
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ENST00000346085.9:c.2808A>C
|
ENSP00000344546.4:p.Pro936=
|
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ENST00000350026.9:c.2769A>C
|
ENSP00000055163.7:p.Pro923=
|
|
ENST00000414678.6:c.1176A>C
|
ENSP00000412835.2:p.Pro392=
|
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ENST00000452544.1:n.865A>C
|
|
|
ENST00000478761.3:c.91A>C
|
|
|
NM_017519.2:c.2769A>C
|
NP_059989.2:p.Pro923=
|
|
NM_020732.3:c.2808A>C
|
NP_065783.3:p.Pro936=
|
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XM_005267069.3:c.2769A>C
|
XP_005267126.2:p.Pro923=
|
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XM_011535984.1:c.1719A>C
|
XP_011534286.1:p.Pro573=
|
|
XM_011535985.1:c.1539A>C
|
XP_011534287.1:p.Pro513=
|
|
XM_011535986.1:c.1299A>C
|
XP_011534288.1:p.Pro433=
|
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XM_011535987.1:c.918A>C
|
XP_011534289.1:p.Pro306=
|
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XM_011535988.1:c.-20+15673A>C
|
XP_011534290.1:n.-20+15673A>C
|
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NM_001346813.1:c.2769A>C
|
NP_001333742.1:p.Pro923=
|
|
NM_001363725.1:c.519A>C
|
NP_001350654.1:p.Pro173=
|
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XM_011535984.2:c.2850A>C
|
XP_011534286.2:p.Pro950=
|
|
XM_011535988.3:c.-20+15673A>C
|
XP_011534290.1:n.-20+15673A>C
|
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XM_017011103.2:c.2850A>C
|
XP_016866592.1:p.Pro950=
|
|
XM_017011104.1:c.2850A>C
|
XP_016866593.1:p.Pro950=
|
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XM_017011105.2:c.2850A>C
|
XP_016866594.1:p.Pro950=
|
|
XM_017011106.2:c.2850A>C
|
XP_016866595.1:p.Pro950=
|
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XM_017011107.2:c.2670A>C
|
XP_016866596.1:p.Pro890=
|
|
XR_002956289.1:n.2933A>C
|
|
|
NM_001363725.2:c.519A>C
|
NP_001350654.1:p.Pro173=
|
|
NM_001371656.1:c.3057A>C
|
NP_001358585.1:p.Pro1019=
|
|
NM_001374820.1:c.3057A>C
|
NP_001361749.1:p.Pro1019=
|
|
NM_001374828.1:c.3018A>C
MANE Select
|
NP_001361757.1:p.Pro1006=
|
|
NM_017519.3:c.3018A>C
|
NP_059989.3:p.Pro1006=
|
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