ENST00000346342.8:c.1327T>G
MANE Select
|
ENSP00000329546.4:p.Phe443Val
|
|
ENST00000346342.7:c.1327T>G
|
ENSP00000329546.3:p.Phe443Val
|
|
ENST00000375581.3:c.1393T>G
|
ENSP00000364731.3:p.Phe465Val
|
|
ENST00000541084.5:c.1141T>G
|
ENSP00000442051.2:p.Phe381Val
|
|
NM_000131.4:c.1393T>G , LRG_554t1:c.1393T>G
|
NP_000122.1:p.Phe465Val
|
|
NM_001267554.1:c.1141T>G
|
NP_001254483.1:p.Phe381Val
|
|
NM_019616.3:c.1327T>G , LRG_554t2:c.1327T>G
|
NP_062562.1:p.Phe443Val
|
|
NR_051961.1:n.1414T>G
|
|
|
XM_006719963.2:c.1186T>G
|
XP_006720026.1:p.Phe396Val
|
|
XM_011537474.1:c.1435T>G
|
XP_011535776.1:p.Phe479Val
|
|
XM_011537475.1:c.1249T>G
|
XP_011535777.1:p.Phe417Val
|
|
XM_011537476.1:c.1087T>G
|
XP_011535778.1:p.Phe363Val
|
|
XM_011537477.1:c.1396T>G
|
XP_011535779.1:p.Phe466Val
|
|
XM_006719963.3:c.1231T>G
|
XP_006720026.2:p.Phe411Val
|
|
XM_011537474.2:c.1480T>G
|
XP_011535776.2:p.Phe494Val
|
|
XM_011537475.2:c.1294T>G
|
XP_011535777.2:p.Phe432Val
|
|
XM_011537476.2:c.1087T>G
|
XP_011535778.1:p.Phe363Val
|
|
NM_019616.4:c.1327T>G
MANE Select
|
NP_062562.1:p.Phe443Val
|
|
NR_051961.2:n.1411T>G
|
|
|
NM_001267554.2:c.1141T>G
|
NP_001254483.1:p.Phe381Val
|
|