ENST00000340850.10:c.408C>T
|
ENSP00000344570.5:p.Tyr136=
|
|
ENST00000377728.8:c.408C>T
MANE Select
|
ENSP00000366957.3:p.Tyr136=
|
|
ENST00000377740.5:c.408C>T
|
ENSP00000366969.4:p.Tyr136=
|
|
ENST00000377748.6:c.582C>T
|
ENSP00000366977.2:p.Tyr194=
|
|
ENST00000400913.6:c.408C>T
|
ENSP00000383704.1:p.Tyr136=
|
|
ENST00000400915.8:c.519C>T
|
ENSP00000383706.4:p.Tyr173=
|
|
ENST00000489097.6:n.884C>T
|
|
|
ENST00000535355.6:c.615C>T
|
ENSP00000441445.1:p.Tyr205=
|
|
ENST00000537245.6:c.519C>T
|
ENSP00000439625.2:p.Tyr173=
|
|
ENST00000673471.2:c.705C>T
|
ENSP00000500749.1:p.Tyr235=
|
|
ENST00000674790.1:c.*620C>T
|
ENSP00000502815.1:n.*620C>T
|
|
ENST00000675123.1:c.408C>T
|
ENSP00000502132.1:p.Tyr136=
|
|
ENST00000675548.1:c.*236C>T
|
ENSP00000502684.1:n.*236C>T
|
|
ENST00000675694.1:c.408C>T
|
ENSP00000501925.1:p.Tyr136=
|
|
ENST00000676255.1:c.370C>T
|
ENSP00000502459.1:n.370C>T
|
|
ENST00000340850.9:c.408C>T
|
ENSP00000344570.5:p.Tyr136=
|
|
ENST00000377725.5:c.408C>T
|
ENSP00000366954.1:p.Tyr136=
|
|
ENST00000377728.7:c.408C>T
|
ENSP00000366957.3:p.Tyr136=
|
|
ENST00000377732.5:c.519C>T
|
ENSP00000366961.1:p.Tyr173=
|
|
ENST00000377740.4:c.639C>T
|
ENSP00000366969.3:p.Tyr213=
|
|
ENST00000377748.5:c.639C>T
|
ENSP00000366977.1:p.Tyr213=
|
|
ENST00000400913.5:c.408C>T
|
ENSP00000383704.1:p.Tyr136=
|
|
ENST00000400915.7:c.576C>T
|
ENSP00000383706.3:p.Tyr192=
|
|
ENST00000489097.5:n.884C>T
|
|
|
ENST00000535355.5:c.615C>T
|
ENSP00000441445.1:p.Tyr205=
|
|
ENST00000537245.5:c.645C>T
|
ENSP00000439625.1:p.Tyr215=
|
|
NM_001042663.1:c.576C>T
|
NP_001036128.1:p.Tyr192=
|
|
NM_001042664.1:c.408C>T
|
NP_001036129.1:p.Tyr136=
|
|
NM_001042665.1:c.408C>T
|
NP_001036130.1:p.Tyr136=
|
|
NM_001265592.1:c.645C>T
|
NP_001252521.1:p.Tyr215=
|
|
NM_001265593.1:c.615C>T
|
NP_001252522.1:p.Tyr205=
|
|
NM_001265594.1:c.408C>T
|
NP_001252523.1:p.Tyr136=
|
|
NM_020631.4:c.408C>T
|
NP_065682.2:p.Tyr136=
|
|
NM_198681.3:c.639C>T
|
NP_941374.2:p.Tyr213=
|
|
NM_001042663.2:c.576C>T
|
NP_001036128.1:p.Tyr192=
|
|
NM_001265594.2:c.408C>T
|
NP_001252523.1:p.Tyr136=
|
|
NM_020631.5:c.408C>T
|
NP_065682.2:p.Tyr136=
|
|
NM_001042663.3:c.519C>T
|
NP_001036128.2:p.Tyr173=
|
|
NM_001265592.2:c.519C>T
|
NP_001252521.2:p.Tyr173=
|
|
NM_020631.6:c.408C>T
MANE Select
|
NP_065682.2:p.Tyr136=
|
|
NM_198681.4:c.408C>T
|
NP_941374.3:p.Tyr136=
|
|