ENST00000696154.2:n.1585T>G
|
|
|
ENST00000696154.1:c.*795T>G
|
ENSP00000512445.1:n.*795T>G
|
|
ENST00000696155.1:n.361T>G
|
|
|
ENST00000259089.9:c.1477T>G
MANE Select
|
ENSP00000259089.4:p.Phe493Val
|
|
ENST00000645242.1:c.1264T>G
|
ENSP00000494690.1:p.Phe422Val
|
|
ENST00000259089.8:c.1477T>G
|
ENSP00000259089.4:p.Phe493Val
|
|
ENST00000526097.1:n.1417T>G
|
|
|
ENST00000529894.1:c.1264T>G
|
ENSP00000433663.1:p.Phe422Val
|
|
NM_001715.2:c.1477T>G
|
NP_001706.2:p.Phe493Val
|
|
XM_011543824.1:c.1555T>G
|
XP_011542126.1:p.Phe519Val
|
|
XM_011543825.1:c.1555T>G
|
XP_011542127.1:p.Phe519Val
|
|
XM_011543826.1:c.1555T>G
|
XP_011542128.1:p.Phe519Val
|
|
XM_011543827.1:c.1342T>G
|
XP_011542129.1:p.Phe448Val
|
|
NM_001330465.1:c.1264T>G
|
NP_001317394.1:p.Phe422Val
|
|
XM_011543825.3:c.1555T>G
|
XP_011542127.1:p.Phe519Val
|
|
NM_001715.3:c.1477T>G
MANE Select
|
NP_001706.2:p.Phe493Val
|
|
NM_001330465.2:c.1264T>G
|
NP_001317394.1:p.Phe422Val
|
|