ENST00000583535.6:c.5804T>C
MANE Select
|
ENSP00000464317.1:p.Val1935Ala
|
|
ENST00000577963.1:n.346T>C
|
|
|
ENST00000579928.2:n.334T>C
|
|
|
ENST00000583535.5:c.5804T>C
|
ENSP00000464317.1:p.Val1935Ala
|
|
NM_002470.3:c.5804T>C
|
NP_002461.2:p.Val1935Ala
|
|
XM_011523870.1:c.5804T>C
|
XP_011522172.1:p.Val1935Ala
|
|
XM_011523871.1:c.5804T>C
|
XP_011522173.1:p.Val1935Ala
|
|
XM_011523870.3:c.5804T>C
|
XP_011522172.1:p.Val1935Ala
|
|
XM_011523871.2:c.5804T>C
|
XP_011522173.1:p.Val1935Ala
|
|
NM_002470.4:c.5804T>C
MANE Select
|
NP_002461.2:p.Val1935Ala
|
|