ENST00000592699.6:c.751G>T
|
ENSP00000466263.1:p.Val251Phe
|
|
ENST00000682485.1:n.1025G>T
|
|
|
ENST00000262093.11:c.850G>T
MANE Select
|
ENSP00000262093.6:p.Val284Phe
|
|
ENST00000382873.8:c.634G>T
|
ENSP00000372326.4:p.Val212Phe
|
|
ENST00000651787.1:n.956G>T
|
|
|
ENST00000651812.1:n.447G>T
|
|
|
ENST00000652755.1:c.868G>T
|
ENSP00000498358.1:p.Val290Phe
|
|
ENST00000262093.9:c.850G>T
|
ENSP00000262093.5:p.Val284Phe
|
|
ENST00000382873.7:c.868G>T
|
ENSP00000372326.3:p.Val290Phe
|
|
ENST00000585494.5:c.*577G>T
|
ENSP00000465243.1:n.*577G>T
|
|
ENST00000591977.5:c.117G>T
|
|
|
ENST00000592699.5:c.751G>T
|
ENSP00000466263.1:p.Val251Phe
|
|
NM_000140.3:c.850G>T
|
NP_000131.2:p.Val284Phe
|
|
NM_001012515.2:c.868G>T
|
NP_001012533.1:p.Val290Phe
|
|
XM_011525881.1:c.769G>T
|
XP_011524183.1:p.Val257Phe
|
|
XM_011525882.1:c.634G>T
|
XP_011524184.1:p.Val212Phe
|
|
NM_000140.4:c.850G>T
|
NP_000131.2:p.Val284Phe
|
|
NM_001012515.3:c.868G>T
|
NP_001012533.1:p.Val290Phe
|
|
XM_011525882.2:c.634G>T
|
XP_011524184.1:p.Val212Phe
|
|
XM_017025614.2:c.751G>T
|
XP_016881103.1:p.Val251Phe
|
|
NM_000140.5:c.850G>T
MANE Select
|
NP_000131.2:p.Val284Phe
|
|
NM_001012515.4:c.868G>T
|
NP_001012533.1:p.Val290Phe
|
|
NM_001371094.1:c.751G>T
|
NP_001358023.1:p.Val251Phe
|
|
NM_001371095.1:c.634G>T
|
NP_001358024.1:p.Val212Phe
|
|
NM_001374778.1:c.850G>T
|
NP_001361707.1:p.Val284Phe
|
|