ENST00000300026.4:c.331G>C
MANE Select
|
ENSP00000300026.4:p.Asp111His
|
|
ENST00000561048.2:n.364G>C
|
|
|
ENST00000680158.1:c.331G>C
|
ENSP00000504873.1:p.Asp111His
|
|
ENST00000680343.1:n.285G>C
|
|
|
ENST00000681397.1:c.331G>C
|
ENSP00000506584.1:p.Asp111His
|
|
ENST00000681658.1:c.226G>C
|
ENSP00000505431.1:p.Asp76His
|
|
ENST00000300026.3:c.331G>C
|
ENSP00000300026.3:p.Asp111His
|
|
ENST00000558492.1:n.237G>C
|
|
|
ENST00000561048.1:n.366G>C
|
|
|
NM_000942.4:c.331G>C , LRG_10t1:c.331G>C
|
NP_000933.1:p.Asp111His
|
|
NM_000942.5:c.331G>C
MANE Select
|
NP_000933.1:p.Asp111His
|
|