ENST00000352511.5:c.1263C>A
MANE Select
|
ENSP00000340361.3:p.His421Gln
|
|
ENST00000352511.4:c.1263C>A
|
ENSP00000340361.3:p.His421Gln
|
|
ENST00000461232.1:n.5052C>A
|
|
|
ENST00000465020.5:n.1349C>A
|
|
|
NM_001106.3:c.1263C>A
|
NP_001097.2:p.His421Gln
|
|
XM_005265583.2:c.1326C>A
|
XP_005265640.1:p.His442Gln
|
|
XM_005265583.3:c.1326C>A
|
XP_005265640.1:p.His442Gln
|
|
XM_017007514.1:c.1305C>A
|
XP_016863003.1:p.His435Gln
|
|
XM_017007515.2:c.1281C>A
|
XP_016863004.1:p.His427Gln
|
|
XM_017007516.1:c.1260C>A
|
XP_016863005.1:p.His420Gln
|
|
NM_001106.4:c.1263C>A
MANE Select
|
NP_001097.2:p.His421Gln
|
|