ENST00000592699.6:c.752T>C
|
ENSP00000466263.1:p.Val251Ala
|
|
ENST00000682485.1:n.1026T>C
|
|
|
ENST00000262093.11:c.851T>C
MANE Select
|
ENSP00000262093.6:p.Val284Ala
|
|
ENST00000382873.8:c.635T>C
|
ENSP00000372326.4:p.Val212Ala
|
|
ENST00000651787.1:n.957T>C
|
|
|
ENST00000651812.1:n.448T>C
|
|
|
ENST00000652755.1:c.869T>C
|
ENSP00000498358.1:p.Val290Ala
|
|
ENST00000262093.9:c.851T>C
|
ENSP00000262093.5:p.Val284Ala
|
|
ENST00000382873.7:c.869T>C
|
ENSP00000372326.3:p.Val290Ala
|
|
ENST00000585494.5:c.*578T>C
|
ENSP00000465243.1:n.*578T>C
|
|
ENST00000591977.5:c.118T>C
|
|
|
ENST00000592699.5:c.752T>C
|
ENSP00000466263.1:p.Val251Ala
|
|
NM_000140.3:c.851T>C
|
NP_000131.2:p.Val284Ala
|
|
NM_001012515.2:c.869T>C
|
NP_001012533.1:p.Val290Ala
|
|
XM_011525881.1:c.770T>C
|
XP_011524183.1:p.Val257Ala
|
|
XM_011525882.1:c.635T>C
|
XP_011524184.1:p.Val212Ala
|
|
NM_000140.4:c.851T>C
|
NP_000131.2:p.Val284Ala
|
|
NM_001012515.3:c.869T>C
|
NP_001012533.1:p.Val290Ala
|
|
XM_011525882.2:c.635T>C
|
XP_011524184.1:p.Val212Ala
|
|
XM_017025614.2:c.752T>C
|
XP_016881103.1:p.Val251Ala
|
|
NM_000140.5:c.851T>C
MANE Select
|
NP_000131.2:p.Val284Ala
|
|
NM_001012515.4:c.869T>C
|
NP_001012533.1:p.Val290Ala
|
|
NM_001371094.1:c.752T>C
|
NP_001358023.1:p.Val251Ala
|
|
NM_001371095.1:c.635T>C
|
NP_001358024.1:p.Val212Ala
|
|
NM_001374778.1:c.851T>C
|
NP_001361707.1:p.Val284Ala
|
|