ENST00000396992.8:c.443G>A
MANE Select
|
ENSP00000380189.3:p.Cys148Tyr
|
|
ENST00000640573.1:n.681G>A
|
|
|
ENST00000247153.7:c.443G>A
|
ENSP00000247153.3:p.Cys148Tyr
|
|
ENST00000377005.6:c.443G>A
|
ENSP00000366204.2:p.Cys148Tyr
|
|
ENST00000396992.7:c.443G>A
|
ENSP00000380189.3:p.Cys148Tyr
|
|
ENST00000469388.1:c.38G>A
|
ENSP00000418258.1:p.Cys13Tyr
|
|
ENST00000485991.5:n.1740G>A
|
|
|
NM_001145252.1:c.443G>A
|
NP_001138724.1:p.Cys148Tyr
|
|
NM_002621.2:c.443G>A , LRG_129t1:c.443G>A
|
NP_002612.1:p.Cys148Tyr
|
|
XM_017029575.1:c.38G>A
|
XP_016885064.1:p.Cys13Tyr
|
|
NM_001145252.3:c.443G>A
MANE Select
|
NP_001138724.1:p.Cys148Tyr
|
|