ENST00000696154.2:n.1598C>G
|
|
|
ENST00000696154.1:c.*808C>G
|
ENSP00000512445.1:n.*808C>G
|
|
ENST00000696155.1:n.374C>G
|
|
|
ENST00000259089.9:c.1490C>G
MANE Select
|
ENSP00000259089.4:p.Thr497Ser
|
|
ENST00000645242.1:c.1277C>G
|
ENSP00000494690.1:p.Thr426Ser
|
|
ENST00000259089.8:c.1490C>G
|
ENSP00000259089.4:p.Thr497Ser
|
|
ENST00000526097.1:n.1430C>G
|
|
|
ENST00000529894.1:c.1277C>G
|
ENSP00000433663.1:p.Thr426Ser
|
|
NM_001715.2:c.1490C>G
|
NP_001706.2:p.Thr497Ser
|
|
XM_011543824.1:c.1568C>G
|
XP_011542126.1:p.Thr523Ser
|
|
XM_011543825.1:c.1568C>G
|
XP_011542127.1:p.Thr523Ser
|
|
XM_011543826.1:c.1568C>G
|
XP_011542128.1:p.Thr523Ser
|
|
XM_011543827.1:c.1355C>G
|
XP_011542129.1:p.Thr452Ser
|
|
NM_001330465.1:c.1277C>G
|
NP_001317394.1:p.Thr426Ser
|
|
XM_011543825.3:c.1568C>G
|
XP_011542127.1:p.Thr523Ser
|
|
NM_001715.3:c.1490C>G
MANE Select
|
NP_001706.2:p.Thr497Ser
|
|
NM_001330465.2:c.1277C>G
|
NP_001317394.1:p.Thr426Ser
|
|