ENST00000456935.7:c.751G>C
MANE Select
|
ENSP00000395473.2:p.Asp251His
|
|
ENST00000221363.8:c.751G>C
|
ENSP00000221363.4:p.Asp251His
|
|
ENST00000456935.6:c.751G>C
|
ENSP00000395473.2:p.Asp251His
|
|
ENST00000466794.5:n.733G>C
|
|
|
ENST00000486847.2:c.454G>C
|
ENSP00000470174.1:p.Asp152His
|
|
NM_000528.3:c.751G>C
|
NP_000519.2:p.Asp251His
|
|
NM_001173498.1:c.751G>C
|
NP_001166969.1:p.Asp251His
|
|
XM_005259913.1:c.751G>C
|
XP_005259970.1:p.Asp251His
|
|
XM_005259913.2:c.751G>C
|
XP_005259970.1:p.Asp251His
|
|
XM_024451518.1:c.-268G>C
|
XP_024307286.1:n.-268G>C
|
|
NM_000528.4:c.751G>C
MANE Select
|
NP_000519.2:p.Asp251His
|
|
NM_001173498.2:c.751G>C
|
NP_001166969.1:p.Asp251His
|
|