ENST00000402696.9:c.1794G>A
MANE Select
|
ENSP00000385834.3:p.Leu598=
|
|
ENST00000402696.7:c.1794G>A
|
ENSP00000385834.3:p.Leu598=
|
|
ENST00000461695.1:c.525G>A
|
|
|
ENST00000467842.1:n.2788G>A
|
|
|
NM_001063.3:c.1794G>A
|
NP_001054.1:p.Leu598=
|
|
XM_011513100.1:c.1794G>A
|
XP_011511402.1:p.Leu598=
|
|
NM_001354703.1:c.1662G>A
|
NP_001341632.1:p.Leu554=
|
|
NM_001354704.1:c.1413G>A
|
NP_001341633.1:p.Leu471=
|
|
NM_001063.4:c.1794G>A
MANE Select
|
NP_001054.2:p.Leu598=
|
|
NM_001354703.2:c.1662G>A
|
NP_001341632.2:p.Leu554=
|
|
NM_001354704.2:c.1413G>A
|
NP_001341633.2:p.Leu471=
|
|