|
NM_000203.5:c.1323C>A
MANE Select
|
NP_000194.2:p.Tyr441Ter
|
|
ENST00000514224.2:c.1323C>A
MANE Select
|
ENSP00000425081.2:p.Tyr441Ter
|
|
NM_000203.4:c.1323C>A
|
NP_000194.2:p.Tyr441Ter
|
|
NM_001363576.1:c.927C>A
|
NP_001350505.1:p.Tyr309Ter
|
|
NR_110313.1:n.1411C>A
|
|
|
ENST00000247933.8:c.1323C>A
|
ENSP00000247933.4:p.Tyr441Ter
|
|
ENST00000247933.9:c.1323C>A
|
ENSP00000247933.4:p.Tyr441Ter
|
|
ENST00000502829.1:n.125C>A
|
|
|
ENST00000514224.1:c.927C>A
|
ENSP00000425081.1:p.Tyr309Ter
|
|
ENST00000514698.5:n.1430C>A
|
|
|
ENST00000652070.1:n.1379C>A
|
|
|
XM_006713882.2:c.927C>A
|
XP_006713945.1:p.Tyr309Ter
|
|
XM_011513459.1:c.1389C>A
|
XP_011511761.1:p.Tyr463Ter
|
|
XM_011513460.1:c.1182C>A
|
XP_011511762.1:p.Tyr394Ter
|
|
XM_011513461.1:c.1116C>A
|
XP_011511763.1:p.Tyr372Ter
|
|
XM_011513461.2:c.1116C>A
|
XP_011511763.1:p.Tyr372Ter
|
|
XM_011513462.1:c.1035C>A
|
XP_011511764.1:p.Tyr345Ter
|
|
XM_011513463.1:c.1035C>A
|
XP_011511765.1:p.Tyr345Ter
|
|
XM_017008163.1:c.363C>A
|
XP_016863652.1:p.Tyr121Ter
|
|
XR_924947.1:n.1392C>A
|
|