ENST00000695527.1:n.18G>T
|
|
|
ENST00000695558.1:c.5706G>T
|
ENSP00000512015.1:p.Leu1902=
|
|
ENST00000703224.1:c.*4916G>T
|
ENSP00000515242.1:n.*4916G>T
|
|
ENST00000359568.10:c.5673G>T
MANE Select
|
ENSP00000352572.5:p.Leu1891=
|
|
ENST00000359568.9:c.5673G>T
|
ENSP00000352572.5:p.Leu1891=
|
|
ENST00000480896.5:n.5942G>T
|
|
|
NM_001315529.1:c.5319G>T
|
NP_001302458.1:p.Leu1773=
|
|
NM_006031.5:c.5673G>T
|
NP_006022.3:p.Leu1891=
|
|
XM_005261124.3:c.5706G>T
|
XP_005261181.1:p.Leu1902=
|
|
XM_011529593.1:c.5784G>T
|
XP_011527895.1:p.Leu1928=
|
|
XM_011529594.1:c.5754G>T
|
XP_011527896.1:p.Leu1918=
|
|
XM_005261124.5:c.5706G>T
|
XP_005261181.1:p.Leu1902=
|
|
XM_011529594.3:c.5754G>T
|
XP_011527896.1:p.Leu1918=
|
|
XM_017028362.2:c.5673G>T
|
XP_016883851.1:p.Leu1891=
|
|
XM_017028363.1:c.5352G>T
|
XP_016883852.1:p.Leu1784=
|
|
XM_024452082.1:c.4590G>T
|
XP_024307850.1:p.Leu1530=
|
|
XM_024452083.1:c.3486G>T
|
XP_024307851.1:p.Leu1162=
|
|
NM_006031.6:c.5673G>T
MANE Select
|
NP_006022.3:p.Leu1891=
|
|
NM_001315529.2:c.5319G>T
|
NP_001302458.1:p.Leu1773=
|
|