|
NM_001361.5:c.73G>A
MANE Select
|
NP_001352.2:p.Ala25Thr
|
|
ENST00000219240.9:c.73G>A
MANE Select
|
ENSP00000219240.4:p.Ala25Thr
|
|
NM_001361.4:c.73G>A
|
NP_001352.2:p.Ala25Thr
|
|
ENST00000219240.8:c.73G>A
|
ENSP00000219240.4:p.Ala25Thr
|
|
ENST00000571288.6:c.60G>A
|
|
|
ENST00000572887.5:c.73G>A
|
ENSP00000461848.1:p.Ala25Thr
|
|
ENST00000574309.5:c.69G>A
|
|
|
ENST00000576145.1:c.-12G>A
|
ENSP00000464333.1:n.-12G>A
|
|
XM_005255827.2:c.-12G>A
|
XP_005255884.1:n.-12G>A
|
|
XM_005255827.4:c.-12G>A
|
XP_005255884.1:n.-12G>A
|
|
XM_017022990.2:c.-356G>A
|
XP_016878479.1:n.-356G>A
|