ENST00000350026.11:c.3831A>T
|
ENSP00000055163.8:p.Pro1277=
|
|
ENST00000414678.8:c.3900A>T
|
ENSP00000412835.3:p.Pro1300=
|
|
ENST00000637015.2:c.4119A>T
|
ENSP00000489729.2:p.Pro1373=
|
|
ENST00000346085.10:c.3870A>T
|
ENSP00000344546.5:p.Pro1290=
|
|
ENST00000350026.10:c.3582A>T
|
ENSP00000055163.7:p.Pro1194=
|
|
ENST00000414678.7:c.2148A>T
|
ENSP00000412835.2:p.Pro716=
|
|
ENST00000635849.1:c.1311A>T
|
ENSP00000490948.1:p.Pro437=
|
|
ENST00000635957.1:c.945A>T
|
ENSP00000490385.1:p.Pro315=
|
|
ENST00000636930.2:c.3990A>T
MANE Select
|
ENSP00000490491.2:p.Pro1330=
|
|
ENST00000636940.1:n.1987A>T
|
|
|
ENST00000637015.1:c.1358A>T
|
|
|
ENST00000637568.1:c.1272A>T
|
|
|
ENST00000637741.1:n.656A>T
|
|
|
ENST00000637810.1:c.1332A>T
|
ENSP00000489636.1:p.Pro444=
|
|
ENST00000637904.1:c.1491A>T
|
ENSP00000490550.1:p.Pro497=
|
|
ENST00000647938.1:c.3621A>T
|
ENSP00000498155.1:p.Pro1207=
|
|
ENST00000346085.9:c.3621A>T
|
ENSP00000344546.4:p.Pro1207=
|
|
ENST00000350026.9:c.3582A>T
|
ENSP00000055163.7:p.Pro1194=
|
|
ENST00000414678.6:c.2148A>T
|
ENSP00000412835.2:p.Pro716=
|
|
NM_017519.2:c.3582A>T
|
NP_059989.2:p.Pro1194=
|
|
NM_020732.3:c.3621A>T
|
NP_065783.3:p.Pro1207=
|
|
XM_005267069.3:c.3741A>T
|
XP_005267126.2:p.Pro1247=
|
|
XM_011535984.1:c.2820A>T
|
XP_011534286.1:p.Pro940=
|
|
XM_011535985.1:c.2640A>T
|
XP_011534287.1:p.Pro880=
|
|
XM_011535986.1:c.2400A>T
|
XP_011534288.1:p.Pro800=
|
|
XM_011535987.1:c.2019A>T
|
XP_011534289.1:p.Pro673=
|
|
XM_011535988.1:c.882A>T
|
XP_011534290.1:p.Pro294=
|
|
NM_001346813.1:c.3741A>T
|
NP_001333742.1:p.Pro1247=
|
|
NM_001363725.1:c.1491A>T
|
NP_001350654.1:p.Pro497=
|
|
XM_011535984.2:c.3951A>T
|
XP_011534286.2:p.Pro1317=
|
|
XM_011535988.3:c.882A>T
|
XP_011534290.1:p.Pro294=
|
|
XM_017011103.2:c.3852A>T
|
XP_016866592.1:p.Pro1284=
|
|
XM_017011104.1:c.3822A>T
|
XP_016866593.1:p.Pro1274=
|
|
XM_017011105.2:c.3792A>T
|
XP_016866594.1:p.Pro1264=
|
|
XM_017011106.2:c.3663A>T
|
XP_016866595.1:p.Pro1221=
|
|
XM_017011107.2:c.3642A>T
|
XP_016866596.1:p.Pro1214=
|
|
XR_002956289.1:n.4034A>T
|
|
|
NM_001363725.2:c.1491A>T
|
NP_001350654.1:p.Pro497=
|
|
NM_001371656.1:c.3870A>T
|
NP_001358585.1:p.Pro1290=
|
|
NM_001374820.1:c.3870A>T
|
NP_001361749.1:p.Pro1290=
|
|
NM_001374828.1:c.3990A>T
MANE Select
|
NP_001361757.1:p.Pro1330=
|
|
NM_017519.3:c.3831A>T
|
NP_059989.3:p.Pro1277=
|
|