ENST00000355808.10:c.642T>C
|
ENSP00000348062.6:p.Ala214=
|
|
ENST00000379805.4:c.*313T>C
|
ENSP00000369133.3:n.*313T>C
|
|
ENST00000417819.6:c.705T>C
|
ENSP00000404616.2:p.Ala235=
|
|
ENST00000423505.6:c.735T>C
|
ENSP00000406473.2:p.Ala245=
|
|
ENST00000481733.2:n.416T>C
|
|
|
ENST00000696704.1:c.436T>C
|
ENSP00000512823.1:p.Leu146=
|
|
ENST00000696705.1:c.*76T>C
|
ENSP00000512824.1:n.*76T>C
|
|
ENST00000422285.7:c.621T>C
MANE Select
|
ENSP00000394382.2:p.Ala207=
|
|
ENST00000379806.9:c.735T>C
|
ENSP00000369134.5:p.Ala245=
|
|
ENST00000422285.6:c.621T>C
|
ENSP00000394382.2:p.Ala207=
|
|
ENST00000479146.1:n.456T>C
|
|
|
ENST00000481733.1:n.49T>C
|
|
|
ENST00000540249.5:c.528T>C
|
ENSP00000440761.1:p.Ala176=
|
|
ENST00000545074.5:c.642T>C
|
ENSP00000438550.1:p.Ala214=
|
|
NM_000284.3:c.621T>C
|
NP_000275.1:p.Ala207=
|
|
NM_001173454.1:c.735T>C
|
NP_001166925.1:p.Ala245=
|
|
NM_001173455.1:c.642T>C
|
NP_001166926.1:p.Ala214=
|
|
NM_001173456.1:c.528T>C
|
NP_001166927.1:p.Ala176=
|
|
XM_011545531.1:c.756T>C
|
XP_011543833.1:p.Ala252=
|
|
XM_011545532.1:c.663T>C
|
XP_011543834.1:p.Ala221=
|
|
XM_017029574.2:c.642T>C
|
XP_016885063.1:p.Ala214=
|
|
NM_000284.4:c.621T>C
MANE Select
|
NP_000275.1:p.Ala207=
|
|
NM_001173454.2:c.735T>C
|
NP_001166925.1:p.Ala245=
|
|
NM_001173455.2:c.642T>C
|
NP_001166926.1:p.Ala214=
|
|
NM_001173456.2:c.528T>C
|
NP_001166927.1:p.Ala176=
|
|