ENST00000367466.4:c.1505A>C
MANE Select
|
ENSP00000356436.3:p.Tyr502Ser
|
|
ENST00000367466.3:c.1505A>C
|
ENSP00000356436.3:p.Tyr502Ser
|
|
NM_001311193.1:c.1325A>C
|
NP_001298122.1:p.Tyr442Ser
|
|
NM_024420.2:c.1505A>C
|
NP_077734.1:p.Tyr502Ser
|
|
XM_005245267.2:c.1394A>C
|
XP_005245324.1:p.Tyr465Ser
|
|
XM_011509641.1:c.1526A>C
|
XP_011507943.1:p.Tyr509Ser
|
|
XM_011509642.1:c.1505A>C
|
XP_011507944.1:p.Tyr502Ser
|
|
XM_011509643.1:c.1505A>C
|
XP_011507945.1:p.Tyr502Ser
|
|
XR_921838.1:n.1477+89A>C
|
|
|
XM_005245267.4:c.1520A>C
|
XP_005245324.2:p.Tyr507Ser
|
|
XM_011509642.2:c.1505A>C
|
XP_011507944.1:p.Tyr502Ser
|
|
NM_001311193.2:c.1325A>C
|
NP_001298122.2:p.Tyr442Ser
|
|
NM_024420.3:c.1505A>C
MANE Select
|
NP_077734.2:p.Tyr502Ser
|
|