ENST00000402696.9:c.825G>T
MANE Select
|
ENSP00000385834.3:p.Met275Ile
|
|
ENST00000402696.7:c.825G>T
|
ENSP00000385834.3:p.Met275Ile
|
|
ENST00000485977.1:c.190G>T
|
ENSP00000418716.1:p.Gly64Trp
|
|
NM_001063.3:c.825G>T
|
NP_001054.1:p.Met275Ile
|
|
XM_011513100.1:c.825G>T
|
XP_011511402.1:p.Met275Ile
|
|
NM_001354703.1:c.693G>T
|
NP_001341632.1:p.Met231Ile
|
|
NM_001354704.1:c.444G>T
|
NP_001341633.1:p.Met148Ile
|
|
NM_001063.4:c.825G>T
MANE Select
|
NP_001054.2:p.Met275Ile
|
|
NM_001354703.2:c.693G>T
|
NP_001341632.2:p.Met231Ile
|
|
NM_001354704.2:c.444G>T
|
NP_001341633.2:p.Met148Ile
|
|