ENST00000442544.7:c.586G>A
MANE Select
|
ENSP00000389140.2:p.Ala196Thr
|
|
ENST00000304775.12:c.387G>A
|
|
|
ENST00000412726.5:c.517G>A
|
ENSP00000397322.2:p.Ala173Thr
|
|
ENST00000442544.6:c.586G>A
|
ENSP00000389140.2:p.Ala196Thr
|
|
ENST00000579349.1:c.507G>A
|
|
|
ENST00000580024.1:n.499G>A
|
|
|
ENST00000581559.1:c.507G>A
|
ENSP00000463463.1:n.507G>A
|
|
NM_005215.3:c.586G>A
|
NP_005206.2:p.Ala196Thr
|
|
XM_011525843.1:c.586G>A
|
XP_011524145.1:p.Ala196Thr
|
|
XM_011525845.1:c.586G>A
|
XP_011524147.1:p.Ala196Thr
|
|
XM_011525846.1:c.586G>A
|
XP_011524148.1:p.Ala196Thr
|
|
XM_017025568.1:c.586G>A
|
XP_016881057.1:p.Ala196Thr
|
|
XM_017025569.1:c.586G>A
|
XP_016881058.1:p.Ala196Thr
|
|
NM_005215.4:c.586G>A
MANE Select
|
NP_005206.2:p.Ala196Thr
|
|