ENST00000350026.11:c.3938T>C
|
ENSP00000055163.8:p.Val1313Ala
|
|
ENST00000414678.8:c.4007T>C
|
ENSP00000412835.3:p.Val1336Ala
|
|
ENST00000637015.2:c.4226T>C
|
ENSP00000489729.2:p.Val1409Ala
|
|
ENST00000346085.10:c.3977T>C
|
ENSP00000344546.5:p.Val1326Ala
|
|
ENST00000350026.10:c.3689T>C
|
ENSP00000055163.7:p.Val1230Ala
|
|
ENST00000414678.7:c.2255T>C
|
ENSP00000412835.2:p.Val752Ala
|
|
ENST00000635849.1:c.1418T>C
|
ENSP00000490948.1:p.Val473Ala
|
|
ENST00000635957.1:c.1049T>C
|
ENSP00000490385.1:p.Val350Ala
|
|
ENST00000636930.2:c.4097T>C
MANE Select
|
ENSP00000490491.2:p.Val1366Ala
|
|
ENST00000636940.1:n.2094T>C
|
|
|
ENST00000637015.1:c.1465T>C
|
|
|
ENST00000637568.1:c.1379T>C
|
|
|
ENST00000637741.1:n.763T>C
|
|
|
ENST00000637810.1:c.1439T>C
|
ENSP00000489636.1:p.Val480Ala
|
|
ENST00000637904.1:c.1598T>C
|
ENSP00000490550.1:p.Val533Ala
|
|
ENST00000647938.1:c.3728T>C
|
ENSP00000498155.1:p.Val1243Ala
|
|
ENST00000346085.9:c.3728T>C
|
ENSP00000344546.4:p.Val1243Ala
|
|
ENST00000350026.9:c.3689T>C
|
ENSP00000055163.7:p.Val1230Ala
|
|
ENST00000414678.6:c.2255T>C
|
ENSP00000412835.2:p.Val752Ala
|
|
NM_017519.2:c.3689T>C
|
NP_059989.2:p.Val1230Ala
|
|
NM_020732.3:c.3728T>C
|
NP_065783.3:p.Val1243Ala
|
|
XM_005267069.3:c.3848T>C
|
XP_005267126.2:p.Val1283Ala
|
|
XM_011535984.1:c.2927T>C
|
XP_011534286.1:p.Val976Ala
|
|
XM_011535985.1:c.2747T>C
|
XP_011534287.1:p.Val916Ala
|
|
XM_011535986.1:c.2507T>C
|
XP_011534288.1:p.Val836Ala
|
|
XM_011535987.1:c.2126T>C
|
XP_011534289.1:p.Val709Ala
|
|
XM_011535988.1:c.989T>C
|
XP_011534290.1:p.Val330Ala
|
|
NM_001346813.1:c.3848T>C
|
NP_001333742.1:p.Val1283Ala
|
|
NM_001363725.1:c.1598T>C
|
NP_001350654.1:p.Val533Ala
|
|
XM_011535984.2:c.4058T>C
|
XP_011534286.2:p.Val1353Ala
|
|
XM_011535988.3:c.989T>C
|
XP_011534290.1:p.Val330Ala
|
|
XM_017011103.2:c.3959T>C
|
XP_016866592.1:p.Val1320Ala
|
|
XM_017011104.1:c.3929T>C
|
XP_016866593.1:p.Val1310Ala
|
|
XM_017011105.2:c.3899T>C
|
XP_016866594.1:p.Val1300Ala
|
|
XM_017011106.2:c.3770T>C
|
XP_016866595.1:p.Val1257Ala
|
|
XM_017011107.2:c.3749T>C
|
XP_016866596.1:p.Val1250Ala
|
|
XR_002956289.1:n.4141T>C
|
|
|
NM_001363725.2:c.1598T>C
|
NP_001350654.1:p.Val533Ala
|
|
NM_001371656.1:c.3977T>C
|
NP_001358585.1:p.Val1326Ala
|
|
NM_001374820.1:c.3977T>C
|
NP_001361749.1:p.Val1326Ala
|
|
NM_001374828.1:c.4097T>C
MANE Select
|
NP_001361757.1:p.Val1366Ala
|
|
NM_017519.3:c.3938T>C
|
NP_059989.3:p.Val1313Ala
|
|