ENST00000350026.11:c.3056T>G
|
ENSP00000055163.8:p.Val1019Gly
|
|
ENST00000414678.8:c.2966T>G
|
ENSP00000412835.3:p.Val989Gly
|
|
ENST00000637015.2:c.3056T>G
|
ENSP00000489729.2:p.Val1019Gly
|
|
ENST00000319584.11:c.1070T>G
|
ENSP00000313006.7:p.Val357Gly
|
|
ENST00000346085.10:c.3095T>G
|
ENSP00000344546.5:p.Val1032Gly
|
|
ENST00000350026.10:c.2807T>G
|
ENSP00000055163.7:p.Val936Gly
|
|
ENST00000414678.7:c.1214T>G
|
ENSP00000412835.2:p.Val405Gly
|
|
ENST00000452544.2:n.957T>G
|
|
|
ENST00000635849.1:c.377T>G
|
ENSP00000490948.1:p.Val126Gly
|
|
ENST00000635957.1:c.11T>G
|
ENSP00000490385.1:p.Val4Gly
|
|
ENST00000636426.1:n.190T>G
|
|
|
ENST00000636930.2:c.3056T>G
MANE Select
|
ENSP00000490491.2:p.Val1019Gly
|
|
ENST00000637015.1:c.295T>G
|
|
|
ENST00000637568.1:c.99T>G
|
|
|
ENST00000637810.1:c.557T>G
|
ENSP00000489636.1:p.Val186Gly
|
|
ENST00000637904.1:c.557T>G
|
ENSP00000490550.1:p.Val186Gly
|
|
ENST00000647938.1:c.2846T>G
|
ENSP00000498155.1:p.Val949Gly
|
|
ENST00000674190.1:n.1805T>G
|
|
|
ENST00000319584.10:c.1073T>G
|
ENSP00000313006.6:p.Val358Gly
|
|
ENST00000346085.9:c.2846T>G
|
ENSP00000344546.4:p.Val949Gly
|
|
ENST00000350026.9:c.2807T>G
|
ENSP00000055163.7:p.Val936Gly
|
|
ENST00000400790.3:c.8T>G
|
ENSP00000383596.3:p.Val3Gly
|
|
ENST00000414678.6:c.1214T>G
|
ENSP00000412835.2:p.Val405Gly
|
|
ENST00000452544.1:n.903T>G
|
|
|
ENST00000478761.3:c.129T>G
|
|
|
NM_017519.2:c.2807T>G
|
NP_059989.2:p.Val936Gly
|
|
NM_020732.3:c.2846T>G
|
NP_065783.3:p.Val949Gly
|
|
XM_005267069.3:c.2807T>G
|
XP_005267126.2:p.Val936Gly
|
|
XM_011535984.1:c.1757T>G
|
XP_011534286.1:p.Val586Gly
|
|
XM_011535985.1:c.1577T>G
|
XP_011534287.1:p.Val526Gly
|
|
XM_011535986.1:c.1337T>G
|
XP_011534288.1:p.Val446Gly
|
|
XM_011535987.1:c.956T>G
|
XP_011534289.1:p.Val319Gly
|
|
XM_011535988.1:c.-20+15711T>G
|
XP_011534290.1:n.-20+15711T>G
|
|
NM_001346813.1:c.2807T>G
|
NP_001333742.1:p.Val936Gly
|
|
NM_001363725.1:c.557T>G
|
NP_001350654.1:p.Val186Gly
|
|
XM_011535984.2:c.2888T>G
|
XP_011534286.2:p.Val963Gly
|
|
XM_011535988.3:c.-20+15711T>G
|
XP_011534290.1:n.-20+15711T>G
|
|
XM_017011103.2:c.2888T>G
|
XP_016866592.1:p.Val963Gly
|
|
XM_017011104.1:c.2888T>G
|
XP_016866593.1:p.Val963Gly
|
|
XM_017011105.2:c.2888T>G
|
XP_016866594.1:p.Val963Gly
|
|
XM_017011106.2:c.2888T>G
|
XP_016866595.1:p.Val963Gly
|
|
XM_017011107.2:c.2708T>G
|
XP_016866596.1:p.Val903Gly
|
|
XR_002956289.1:n.2971T>G
|
|
|
NM_001363725.2:c.557T>G
|
NP_001350654.1:p.Val186Gly
|
|
NM_001371656.1:c.3095T>G
|
NP_001358585.1:p.Val1032Gly
|
|
NM_001374820.1:c.3095T>G
|
NP_001361749.1:p.Val1032Gly
|
|
NM_001374828.1:c.3056T>G
MANE Select
|
NP_001361757.1:p.Val1019Gly
|
|
NM_017519.3:c.3056T>G
|
NP_059989.3:p.Val1019Gly
|
|