ENST00000322953.9:c.1116T>A
MANE Select
|
ENSP00000320509.4:p.Ser372=
|
|
ENST00000322953.8:c.1116T>A
|
ENSP00000320509.4:p.Ser372=
|
|
ENST00000428908.5:c.717T>A
|
ENSP00000412748.1:p.Ser239=
|
|
ENST00000444316.2:c.1026T>A
|
ENSP00000388817.2:p.Ser342=
|
|
ENST00000504592.5:c.1071T>A
|
ENSP00000421443.1:p.Ser357=
|
|
ENST00000508653.5:c.717T>A
|
ENSP00000422314.1:p.Ser239=
|
|
NM_001083907.2:c.1026T>A
|
NP_001077376.2:p.Ser342=
|
|
NM_001127507.2:c.717T>A
|
NP_001120979.2:p.Ser239=
|
|
NM_017935.4:c.1116T>A
|
NP_060405.4:p.Ser372=
|
|
XM_017008337.2:c.1026T>A
|
XP_016863826.1:p.Ser342=
|
|
NM_017935.5:c.1116T>A
MANE Select
|
NP_060405.5:p.Ser372=
|
|
NM_001083907.3:c.1026T>A
|
NP_001077376.3:p.Ser342=
|
|
NM_001127507.3:c.717T>A
|
NP_001120979.3:p.Ser239=
|
|