ENST00000350026.11:c.3794C>A
|
ENSP00000055163.8:p.Pro1265His
|
|
ENST00000414678.8:c.3863C>A
|
ENSP00000412835.3:p.Pro1288His
|
|
ENST00000637015.2:c.4082C>A
|
ENSP00000489729.2:p.Pro1361His
|
|
ENST00000346085.10:c.3833C>A
|
ENSP00000344546.5:p.Pro1278His
|
|
ENST00000350026.10:c.3545C>A
|
ENSP00000055163.7:p.Pro1182His
|
|
ENST00000414678.7:c.2111C>A
|
ENSP00000412835.2:p.Pro704His
|
|
ENST00000635849.1:c.1274C>A
|
ENSP00000490948.1:p.Pro425His
|
|
ENST00000635957.1:c.908C>A
|
ENSP00000490385.1:p.Pro303His
|
|
ENST00000636930.2:c.3953C>A
MANE Select
|
ENSP00000490491.2:p.Pro1318His
|
|
ENST00000636940.1:n.1950C>A
|
|
|
ENST00000637015.1:c.1321C>A
|
|
|
ENST00000637568.1:c.1235C>A
|
|
|
ENST00000637741.1:n.619C>A
|
|
|
ENST00000637810.1:c.1295C>A
|
ENSP00000489636.1:p.Pro432His
|
|
ENST00000637904.1:c.1454C>A
|
ENSP00000490550.1:p.Pro485His
|
|
ENST00000647938.1:c.3584C>A
|
ENSP00000498155.1:p.Pro1195His
|
|
ENST00000346085.9:c.3584C>A
|
ENSP00000344546.4:p.Pro1195His
|
|
ENST00000350026.9:c.3545C>A
|
ENSP00000055163.7:p.Pro1182His
|
|
ENST00000414678.6:c.2111C>A
|
ENSP00000412835.2:p.Pro704His
|
|
NM_017519.2:c.3545C>A
|
NP_059989.2:p.Pro1182His
|
|
NM_020732.3:c.3584C>A
|
NP_065783.3:p.Pro1195His
|
|
XM_005267069.3:c.3704C>A
|
XP_005267126.2:p.Pro1235His
|
|
XM_011535984.1:c.2783C>A
|
XP_011534286.1:p.Pro928His
|
|
XM_011535985.1:c.2603C>A
|
XP_011534287.1:p.Pro868His
|
|
XM_011535986.1:c.2363C>A
|
XP_011534288.1:p.Pro788His
|
|
XM_011535987.1:c.1982C>A
|
XP_011534289.1:p.Pro661His
|
|
XM_011535988.1:c.845C>A
|
XP_011534290.1:p.Pro282His
|
|
NM_001346813.1:c.3704C>A
|
NP_001333742.1:p.Pro1235His
|
|
NM_001363725.1:c.1454C>A
|
NP_001350654.1:p.Pro485His
|
|
XM_011535984.2:c.3914C>A
|
XP_011534286.2:p.Pro1305His
|
|
XM_011535988.3:c.845C>A
|
XP_011534290.1:p.Pro282His
|
|
XM_017011103.2:c.3815C>A
|
XP_016866592.1:p.Pro1272His
|
|
XM_017011104.1:c.3785C>A
|
XP_016866593.1:p.Pro1262His
|
|
XM_017011105.2:c.3755C>A
|
XP_016866594.1:p.Pro1252His
|
|
XM_017011106.2:c.3626C>A
|
XP_016866595.1:p.Pro1209His
|
|
XM_017011107.2:c.3605C>A
|
XP_016866596.1:p.Pro1202His
|
|
XR_002956289.1:n.3997C>A
|
|
|
NM_001363725.2:c.1454C>A
|
NP_001350654.1:p.Pro485His
|
|
NM_001371656.1:c.3833C>A
|
NP_001358585.1:p.Pro1278His
|
|
NM_001374820.1:c.3833C>A
|
NP_001361749.1:p.Pro1278His
|
|
NM_001374828.1:c.3953C>A
MANE Select
|
NP_001361757.1:p.Pro1318His
|
|
NM_017519.3:c.3794C>A
|
NP_059989.3:p.Pro1265His
|
|