ENST00000350026.11:c.3978A>G
|
ENSP00000055163.8:p.Pro1326=
|
|
ENST00000414678.8:c.4047A>G
|
ENSP00000412835.3:p.Pro1349=
|
|
ENST00000637015.2:c.4266A>G
|
ENSP00000489729.2:p.Pro1422=
|
|
ENST00000346085.10:c.4017A>G
|
ENSP00000344546.5:p.Pro1339=
|
|
ENST00000350026.10:c.3729A>G
|
ENSP00000055163.7:p.Pro1243=
|
|
ENST00000414678.7:c.2295A>G
|
ENSP00000412835.2:p.Pro765=
|
|
ENST00000635849.1:c.1458A>G
|
ENSP00000490948.1:p.Pro486=
|
|
ENST00000635957.1:c.1089A>G
|
ENSP00000490385.1:p.Pro363=
|
|
ENST00000636930.2:c.4137A>G
MANE Select
|
ENSP00000490491.2:p.Pro1379=
|
|
ENST00000636940.1:n.2134A>G
|
|
|
ENST00000637015.1:c.1505A>G
|
|
|
ENST00000637568.1:c.1419A>G
|
|
|
ENST00000637741.1:n.803A>G
|
|
|
ENST00000637810.1:c.1479A>G
|
ENSP00000489636.1:p.Pro493=
|
|
ENST00000637904.1:c.1638A>G
|
ENSP00000490550.1:p.Pro546=
|
|
ENST00000647938.1:c.3768A>G
|
ENSP00000498155.1:p.Pro1256=
|
|
ENST00000346085.9:c.3768A>G
|
ENSP00000344546.4:p.Pro1256=
|
|
ENST00000350026.9:c.3729A>G
|
ENSP00000055163.7:p.Pro1243=
|
|
ENST00000414678.6:c.2295A>G
|
ENSP00000412835.2:p.Pro765=
|
|
NM_017519.2:c.3729A>G
|
NP_059989.2:p.Pro1243=
|
|
NM_020732.3:c.3768A>G
|
NP_065783.3:p.Pro1256=
|
|
XM_005267069.3:c.3888A>G
|
XP_005267126.2:p.Pro1296=
|
|
XM_011535984.1:c.2967A>G
|
XP_011534286.1:p.Pro989=
|
|
XM_011535985.1:c.2787A>G
|
XP_011534287.1:p.Pro929=
|
|
XM_011535986.1:c.2547A>G
|
XP_011534288.1:p.Pro849=
|
|
XM_011535987.1:c.2166A>G
|
XP_011534289.1:p.Pro722=
|
|
XM_011535988.1:c.1029A>G
|
XP_011534290.1:p.Pro343=
|
|
NM_001346813.1:c.3888A>G
|
NP_001333742.1:p.Pro1296=
|
|
NM_001363725.1:c.1638A>G
|
NP_001350654.1:p.Pro546=
|
|
XM_011535984.2:c.4098A>G
|
XP_011534286.2:p.Pro1366=
|
|
XM_011535988.3:c.1029A>G
|
XP_011534290.1:p.Pro343=
|
|
XM_017011103.2:c.3999A>G
|
XP_016866592.1:p.Pro1333=
|
|
XM_017011104.1:c.3969A>G
|
XP_016866593.1:p.Pro1323=
|
|
XM_017011105.2:c.3939A>G
|
XP_016866594.1:p.Pro1313=
|
|
XM_017011106.2:c.3810A>G
|
XP_016866595.1:p.Pro1270=
|
|
XM_017011107.2:c.3789A>G
|
XP_016866596.1:p.Pro1263=
|
|
XR_002956289.1:n.4181A>G
|
|
|
NM_001363725.2:c.1638A>G
|
NP_001350654.1:p.Pro546=
|
|
NM_001371656.1:c.4017A>G
|
NP_001358585.1:p.Pro1339=
|
|
NM_001374820.1:c.4017A>G
|
NP_001361749.1:p.Pro1339=
|
|
NM_001374828.1:c.4137A>G
MANE Select
|
NP_001361757.1:p.Pro1379=
|
|
NM_017519.3:c.3978A>G
|
NP_059989.3:p.Pro1326=
|
|