ENST00000350026.11:c.2951G>T
|
ENSP00000055163.8:p.Ser984Ile
|
|
ENST00000414678.8:c.2861G>T
|
ENSP00000412835.3:p.Ser954Ile
|
|
ENST00000637015.2:c.2951G>T
|
ENSP00000489729.2:p.Ser984Ile
|
|
ENST00000319584.11:c.965G>T
|
ENSP00000313006.7:p.Ser322Ile
|
|
ENST00000346085.10:c.2990G>T
|
ENSP00000344546.5:p.Ser997Ile
|
|
ENST00000350026.10:c.2702G>T
|
ENSP00000055163.7:p.Ser901Ile
|
|
ENST00000414678.7:c.1109G>T
|
ENSP00000412835.2:p.Ser370Ile
|
|
ENST00000452544.2:n.852G>T
|
|
|
ENST00000635849.1:c.272G>T
|
ENSP00000490948.1:p.Ser91Ile
|
|
ENST00000636426.1:n.85G>T
|
|
|
ENST00000636930.2:c.2951G>T
MANE Select
|
ENSP00000490491.2:p.Ser984Ile
|
|
ENST00000637015.1:c.190G>T
|
|
|
ENST00000637810.1:c.452G>T
|
ENSP00000489636.1:p.Ser151Ile
|
|
ENST00000637904.1:c.452G>T
|
ENSP00000490550.1:p.Ser151Ile
|
|
ENST00000647938.1:c.2741G>T
|
ENSP00000498155.1:p.Ser914Ile
|
|
ENST00000674190.1:n.1700G>T
|
|
|
ENST00000319584.10:c.968G>T
|
ENSP00000313006.6:p.Ser323Ile
|
|
ENST00000346085.9:c.2741G>T
|
ENSP00000344546.4:p.Ser914Ile
|
|
ENST00000350026.9:c.2702G>T
|
ENSP00000055163.7:p.Ser901Ile
|
|
ENST00000414678.6:c.1109G>T
|
ENSP00000412835.2:p.Ser370Ile
|
|
ENST00000452544.1:n.798G>T
|
|
|
ENST00000478761.3:c.24G>T
|
|
|
NM_017519.2:c.2702G>T
|
NP_059989.2:p.Ser901Ile
|
|
NM_020732.3:c.2741G>T
|
NP_065783.3:p.Ser914Ile
|
|
XM_005267069.3:c.2702G>T
|
XP_005267126.2:p.Ser901Ile
|
|
XM_011535984.1:c.1652G>T
|
XP_011534286.1:p.Ser551Ile
|
|
XM_011535985.1:c.1472G>T
|
XP_011534287.1:p.Ser491Ile
|
|
XM_011535986.1:c.1232G>T
|
XP_011534288.1:p.Ser411Ile
|
|
XM_011535987.1:c.851G>T
|
XP_011534289.1:p.Ser284Ile
|
|
XM_011535988.1:c.-20+15606G>T
|
XP_011534290.1:n.-20+15606G>T
|
|
NM_001346813.1:c.2702G>T
|
NP_001333742.1:p.Ser901Ile
|
|
NM_001363725.1:c.452G>T
|
NP_001350654.1:p.Ser151Ile
|
|
XM_011535984.2:c.2783G>T
|
XP_011534286.2:p.Ser928Ile
|
|
XM_011535988.3:c.-20+15606G>T
|
XP_011534290.1:n.-20+15606G>T
|
|
XM_017011103.2:c.2783G>T
|
XP_016866592.1:p.Ser928Ile
|
|
XM_017011104.1:c.2783G>T
|
XP_016866593.1:p.Ser928Ile
|
|
XM_017011105.2:c.2783G>T
|
XP_016866594.1:p.Ser928Ile
|
|
XM_017011106.2:c.2783G>T
|
XP_016866595.1:p.Ser928Ile
|
|
XM_017011107.2:c.2603G>T
|
XP_016866596.1:p.Ser868Ile
|
|
XR_002956289.1:n.2866G>T
|
|
|
NM_001363725.2:c.452G>T
|
NP_001350654.1:p.Ser151Ile
|
|
NM_001371656.1:c.2990G>T
|
NP_001358585.1:p.Ser997Ile
|
|
NM_001374820.1:c.2990G>T
|
NP_001361749.1:p.Ser997Ile
|
|
NM_001374828.1:c.2951G>T
MANE Select
|
NP_001361757.1:p.Ser984Ile
|
|
NM_017519.3:c.2951G>T
|
NP_059989.3:p.Ser984Ile
|
|