ENST00000350026.11:c.3927A>T
|
ENSP00000055163.8:p.Pro1309=
|
|
ENST00000414678.8:c.3996A>T
|
ENSP00000412835.3:p.Pro1332=
|
|
ENST00000637015.2:c.4215A>T
|
ENSP00000489729.2:p.Pro1405=
|
|
ENST00000346085.10:c.3966A>T
|
ENSP00000344546.5:p.Pro1322=
|
|
ENST00000350026.10:c.3678A>T
|
ENSP00000055163.7:p.Pro1226=
|
|
ENST00000414678.7:c.2244A>T
|
ENSP00000412835.2:p.Pro748=
|
|
ENST00000635849.1:c.1407A>T
|
ENSP00000490948.1:p.Pro469=
|
|
ENST00000635957.1:c.1038A>T
|
ENSP00000490385.1:p.Pro346=
|
|
ENST00000636930.2:c.4086A>T
MANE Select
|
ENSP00000490491.2:p.Pro1362=
|
|
ENST00000636940.1:n.2083A>T
|
|
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ENST00000637015.1:c.1454A>T
|
|
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ENST00000637568.1:c.1368A>T
|
|
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ENST00000637741.1:n.752A>T
|
|
|
ENST00000637810.1:c.1428A>T
|
ENSP00000489636.1:p.Pro476=
|
|
ENST00000637904.1:c.1587A>T
|
ENSP00000490550.1:p.Pro529=
|
|
ENST00000647938.1:c.3717A>T
|
ENSP00000498155.1:p.Pro1239=
|
|
ENST00000346085.9:c.3717A>T
|
ENSP00000344546.4:p.Pro1239=
|
|
ENST00000350026.9:c.3678A>T
|
ENSP00000055163.7:p.Pro1226=
|
|
ENST00000414678.6:c.2244A>T
|
ENSP00000412835.2:p.Pro748=
|
|
NM_017519.2:c.3678A>T
|
NP_059989.2:p.Pro1226=
|
|
NM_020732.3:c.3717A>T
|
NP_065783.3:p.Pro1239=
|
|
XM_005267069.3:c.3837A>T
|
XP_005267126.2:p.Pro1279=
|
|
XM_011535984.1:c.2916A>T
|
XP_011534286.1:p.Pro972=
|
|
XM_011535985.1:c.2736A>T
|
XP_011534287.1:p.Pro912=
|
|
XM_011535986.1:c.2496A>T
|
XP_011534288.1:p.Pro832=
|
|
XM_011535987.1:c.2115A>T
|
XP_011534289.1:p.Pro705=
|
|
XM_011535988.1:c.978A>T
|
XP_011534290.1:p.Pro326=
|
|
NM_001346813.1:c.3837A>T
|
NP_001333742.1:p.Pro1279=
|
|
NM_001363725.1:c.1587A>T
|
NP_001350654.1:p.Pro529=
|
|
XM_011535984.2:c.4047A>T
|
XP_011534286.2:p.Pro1349=
|
|
XM_011535988.3:c.978A>T
|
XP_011534290.1:p.Pro326=
|
|
XM_017011103.2:c.3948A>T
|
XP_016866592.1:p.Pro1316=
|
|
XM_017011104.1:c.3918A>T
|
XP_016866593.1:p.Pro1306=
|
|
XM_017011105.2:c.3888A>T
|
XP_016866594.1:p.Pro1296=
|
|
XM_017011106.2:c.3759A>T
|
XP_016866595.1:p.Pro1253=
|
|
XM_017011107.2:c.3738A>T
|
XP_016866596.1:p.Pro1246=
|
|
XR_002956289.1:n.4130A>T
|
|
|
NM_001363725.2:c.1587A>T
|
NP_001350654.1:p.Pro529=
|
|
NM_001371656.1:c.3966A>T
|
NP_001358585.1:p.Pro1322=
|
|
NM_001374820.1:c.3966A>T
|
NP_001361749.1:p.Pro1322=
|
|
NM_001374828.1:c.4086A>T
MANE Select
|
NP_001361757.1:p.Pro1362=
|
|
NM_017519.3:c.3927A>T
|
NP_059989.3:p.Pro1309=
|
|