ENST00000371820.4:c.5149G>T
|
ENSP00000360885.4:p.Asp1717Tyr
|
|
ENST00000371817.8:c.5149G>T
MANE Select
|
ENSP00000360882.3:p.Asp1717Tyr
|
|
ENST00000371817.7:c.5149G>T
|
ENSP00000360882.3:p.Asp1717Tyr
|
|
ENST00000371820.3:c.407G>T
|
|
|
ENST00000618395.4:c.5149G>T
|
ENSP00000481360.1:p.Asp1717Tyr
|
|
NM_000093.4:c.5149G>T
|
NP_000084.3:p.Asp1717Tyr
|
|
NM_001278074.1:c.5149G>T
|
NP_001265003.1:p.Asp1717Tyr
|
|
NR_103451.2:n.71-14774C>A
|
|
|
XR_929712.1:n.5833G>T
|
|
|
XR_929713.1:n.5701G>T
|
|
|
NM_000093.5:c.5149G>T
MANE Select
|
NP_000084.3:p.Asp1717Tyr
|
|