ENST00000247933.9:c.1237G>T
|
ENSP00000247933.4:p.Asp413Tyr
|
|
ENST00000514224.2:c.1237G>T
MANE Select
|
ENSP00000425081.2:p.Asp413Tyr
|
|
ENST00000652070.1:n.1293G>T
|
|
|
ENST00000247933.8:c.1237G>T
|
ENSP00000247933.4:p.Asp413Tyr
|
|
ENST00000502829.1:n.39G>T
|
|
|
ENST00000514224.1:c.841G>T
|
ENSP00000425081.1:p.Asp281Tyr
|
|
ENST00000514698.5:n.1344G>T
|
|
|
NM_000203.4:c.1237G>T
|
NP_000194.2:p.Asp413Tyr
|
|
NR_110313.1:n.1325G>T
|
|
|
XM_006713882.2:c.841G>T
|
XP_006713945.1:p.Asp281Tyr
|
|
XM_011513459.1:c.1303G>T
|
XP_011511761.1:p.Asp435Tyr
|
|
XM_011513460.1:c.1096G>T
|
XP_011511762.1:p.Asp366Tyr
|
|
XM_011513461.1:c.1030G>T
|
XP_011511763.1:p.Asp344Tyr
|
|
XM_011513462.1:c.949G>T
|
XP_011511764.1:p.Asp317Tyr
|
|
XM_011513463.1:c.949G>T
|
XP_011511765.1:p.Asp317Tyr
|
|
XR_924947.1:n.1306G>T
|
|
|
NM_000203.5:c.1237G>T
MANE Select
|
NP_000194.2:p.Asp413Tyr
|
|
NM_001363576.1:c.841G>T
|
NP_001350505.1:p.Asp281Tyr
|
|
XM_011513461.2:c.1030G>T
|
XP_011511763.1:p.Asp344Tyr
|
|
XM_017008163.1:c.277G>T
|
XP_016863652.1:p.Asp93Tyr
|
|