ENST00000402696.9:c.1831G>C
MANE Select
|
ENSP00000385834.3:p.Asp611His
|
|
ENST00000402696.7:c.1831G>C
|
ENSP00000385834.3:p.Asp611His
|
|
ENST00000461695.1:c.562G>C
|
|
|
ENST00000467842.1:n.2825G>C
|
|
|
NM_001063.3:c.1831G>C
|
NP_001054.1:p.Asp611His
|
|
XM_011513100.1:c.1831G>C
|
XP_011511402.1:p.Asp611His
|
|
NM_001354703.1:c.1699G>C
|
NP_001341632.1:p.Asp567His
|
|
NM_001354704.1:c.1450G>C
|
NP_001341633.1:p.Asp484His
|
|
NM_001063.4:c.1831G>C
MANE Select
|
NP_001054.2:p.Asp611His
|
|
NM_001354703.2:c.1699G>C
|
NP_001341632.2:p.Asp567His
|
|
NM_001354704.2:c.1450G>C
|
NP_001341633.2:p.Asp484His
|
|