ENST00000695527.1:n.17T>G
|
|
|
ENST00000695558.1:c.5705T>G
|
ENSP00000512015.1:p.Leu1902Arg
|
|
ENST00000703224.1:c.*4915T>G
|
ENSP00000515242.1:n.*4915T>G
|
|
ENST00000359568.10:c.5672T>G
MANE Select
|
ENSP00000352572.5:p.Leu1891Arg
|
|
ENST00000359568.9:c.5672T>G
|
ENSP00000352572.5:p.Leu1891Arg
|
|
ENST00000480896.5:n.5941T>G
|
|
|
NM_001315529.1:c.5318T>G
|
NP_001302458.1:p.Leu1773Arg
|
|
NM_006031.5:c.5672T>G
|
NP_006022.3:p.Leu1891Arg
|
|
XM_005261124.3:c.5705T>G
|
XP_005261181.1:p.Leu1902Arg
|
|
XM_011529593.1:c.5783T>G
|
XP_011527895.1:p.Leu1928Arg
|
|
XM_011529594.1:c.5753T>G
|
XP_011527896.1:p.Leu1918Arg
|
|
XM_005261124.5:c.5705T>G
|
XP_005261181.1:p.Leu1902Arg
|
|
XM_011529594.3:c.5753T>G
|
XP_011527896.1:p.Leu1918Arg
|
|
XM_017028362.2:c.5672T>G
|
XP_016883851.1:p.Leu1891Arg
|
|
XM_017028363.1:c.5351T>G
|
XP_016883852.1:p.Leu1784Arg
|
|
XM_024452082.1:c.4589T>G
|
XP_024307850.1:p.Leu1530Arg
|
|
XM_024452083.1:c.3485T>G
|
XP_024307851.1:p.Leu1162Arg
|
|
NM_006031.6:c.5672T>G
MANE Select
|
NP_006022.3:p.Leu1891Arg
|
|
NM_001315529.2:c.5318T>G
|
NP_001302458.1:p.Leu1773Arg
|
|