ENST00000324662.8:c.1403T>G
|
ENSP00000313419.4:p.Leu468Arg
|
|
ENST00000538922.8:c.1403T>G
MANE Select
|
ENSP00000437940.2:p.Leu468Arg
|
|
ENST00000324662.7:c.1403T>G
|
ENSP00000313419.3:p.Leu468Arg
|
|
ENST00000538922.5:c.1403T>G
|
ENSP00000437940.1:p.Leu468Arg
|
|
ENST00000565089.5:n.1837T>G
|
|
|
ENST00000567368.1:n.543T>G
|
|
|
ENST00000567541.5:c.1403T>G
|
ENSP00000456201.1:p.Leu468Arg
|
|
ENST00000611258.4:c.1402T>G
|
ENSP00000481090.1:p.Ter468Gly
|
|
NM_001178098.1:c.1403T>G
|
NP_001171569.1:p.Leu468Arg
|
|
NM_001770.5:c.1403T>G , LRG_35t1:c.1403T>G
|
NP_001761.3:p.Leu468Arg
|
|
XM_006721103.2:c.1136T>G
|
XP_006721166.1:p.Leu379Arg
|
|
XM_006721103.3:c.1136T>G
|
XP_006721166.1:p.Leu379Arg
|
|
XM_017023893.1:c.1136T>G
|
XP_016879382.1:p.Leu379Arg
|
|
NM_001178098.2:c.1403T>G
|
NP_001171569.1:p.Leu468Arg
|
|
NM_001770.6:c.1403T>G
MANE Select
|
NP_001761.3:p.Leu468Arg
|
|
NM_001385732.1:c.1136T>G
|
NP_001372661.1:p.Leu379Arg
|
|
NR_169755.1:n.1745T>G
|
|
|