|
NM_004409.5:c.1267C>G
MANE Select
|
NP_004400.4:p.Leu423Val
|
|
ENST00000291270.9:c.1267C>G
MANE Select
|
ENSP00000291270.4:p.Leu423Val
|
|
NM_001081560.2:c.1252C>G
|
NP_001075029.1:p.Leu418Val
|
|
NM_001081560.3:c.1252C>G
|
NP_001075029.1:p.Leu418Val
|
|
NM_001081562.2:c.1252C>G
|
NP_001075031.1:p.Leu418Val
|
|
NM_001081562.3:c.1252C>G
|
NP_001075031.1:p.Leu418Val
|
|
NM_001081563.2:c.1297C>G
|
NP_001075032.1:p.Leu433Val
|
|
NM_001288764.1:c.1345C>G
|
NP_001275693.1:p.Leu449Val
|
|
NM_001288764.2:c.1345C>G
|
NP_001275693.1:p.Leu449Val
|
|
NM_001288765.1:c.1000C>G
|
NP_001275694.1:p.Leu334Val
|
|
NM_001288765.2:c.1000C>G
|
NP_001275694.1:p.Leu334Val
|
|
NM_001288766.1:c.1252C>G
|
NP_001275695.1:p.Leu418Val
|
|
NM_001288766.2:c.1252C>G
|
NP_001275695.1:p.Leu418Val
|
|
NM_004409.4:c.1267C>G
|
NP_004400.4:p.Leu423Val
|
|
ENST00000291270.8:c.1267C>G
|
ENSP00000291270.3:p.Leu423Val
|
|
ENST00000343373.10:c.1267C>G
|
ENSP00000345997.4:p.Leu423Val
|
|
ENST00000343373.8:c.1297C>G
|
ENSP00000345997.3:p.Leu433Val
|
|
ENST00000343373.9:c.1297C>G
|
ENSP00000345997.3:p.Leu433Val
|
|
ENST00000354227.9:c.1252C>G
|
ENSP00000346168.5:p.Leu418Val
|
|
ENST00000447742.6:c.1252C>G
|
ENSP00000413417.1:p.Leu418Val
|
|
ENST00000458663.6:c.1252C>G
|
ENSP00000401753.1:p.Leu418Val
|
|
ENST00000588522.5:c.*1089C>G
|
ENSP00000468013.1:n.*1089C>G
|
|
ENST00000593574.1:c.242C>G
|
|
|
ENST00000596686.5:n.1112C>G
|
|
|
ENST00000600370.1:n.355C>G
|
|
|
ENST00000600370.2:n.1089C>G
|
|
|
ENST00000600757.5:c.1282C>G
|
ENSP00000472965.1:p.Leu428Val
|
|
ENST00000600757.6:n.1841C>G
|
|
|
ENST00000618091.4:c.1252C>G
|
ENSP00000482746.1:p.Leu418Val
|
|
ENST00000674226.1:n.1970C>G
|
|
|
ENST00000682259.1:n.1783C>G
|
|
|
ENST00000682335.1:n.1841C>G
|
|
|
ENST00000682436.1:n.134C>G
|
|
|
ENST00000682994.1:n.2695C>G
|
|
|
ENST00000683086.1:c.1267C>G
|
ENSP00000508381.1:p.Leu423Val
|
|
ENST00000683830.1:n.2176C>G
|
|
|
ENST00000684007.1:n.1574C>G
|
|
|
ENST00000684672.1:n.1618C>G
|
|
