ENST00000696154.2:n.1527G>A
|
|
|
ENST00000696154.1:c.*737G>A
|
ENSP00000512445.1:n.*737G>A
|
|
ENST00000696155.1:n.303G>A
|
|
|
ENST00000259089.9:c.1419G>A
MANE Select
|
ENSP00000259089.4:p.Trp473Ter
|
|
ENST00000645242.1:c.1206G>A
|
ENSP00000494690.1:p.Trp402Ter
|
|
ENST00000259089.8:c.1419G>A
|
ENSP00000259089.4:p.Trp473Ter
|
|
ENST00000526097.1:n.1359G>A
|
|
|
ENST00000529894.1:c.1206G>A
|
ENSP00000433663.1:p.Trp402Ter
|
|
NM_001715.2:c.1419G>A
|
NP_001706.2:p.Trp473Ter
|
|
XM_011543824.1:c.1497G>A
|
XP_011542126.1:p.Trp499Ter
|
|
XM_011543825.1:c.1497G>A
|
XP_011542127.1:p.Trp499Ter
|
|
XM_011543826.1:c.1497G>A
|
XP_011542128.1:p.Trp499Ter
|
|
XM_011543827.1:c.1284G>A
|
XP_011542129.1:p.Trp428Ter
|
|
NM_001330465.1:c.1206G>A
|
NP_001317394.1:p.Trp402Ter
|
|
XM_011543825.3:c.1497G>A
|
XP_011542127.1:p.Trp499Ter
|
|
NM_001715.3:c.1419G>A
MANE Select
|
NP_001706.2:p.Trp473Ter
|
|
NM_001330465.2:c.1206G>A
|
NP_001317394.1:p.Trp402Ter
|
|