ENST00000646743.1:c.170A>T
MANE Select
|
ENSP00000495564.1:p.Asp57Val
|
|
ENST00000251808.7:c.170A>T
|
ENSP00000251808.3:p.Asp57Val
|
|
ENST00000395927.1:c.122A>T
|
ENSP00000379260.1:p.Asp41Val
|
|
ENST00000472106.2:n.498A>T
|
|
|
NM_024915.3:c.170A>T
|
NP_079191.2:p.Asp57Val
|
|
XM_011517305.1:c.122A>T
|
XP_011515607.1:p.Asp41Val
|
|
XM_011517306.1:c.122A>T
|
XP_011515608.1:p.Asp41Val
|
|
XM_011517307.1:c.170A>T
|
XP_011515609.1:p.Asp57Val
|
|
NM_001330593.1:c.122A>T
|
NP_001317522.1:p.Asp41Val
|
|
XM_011517306.3:c.122A>T
|
XP_011515608.1:p.Asp41Val
|
|
XM_011517307.3:c.170A>T
|
XP_011515609.1:p.Asp57Val
|
|
NM_001330593.2:c.122A>T
|
NP_001317522.1:p.Asp41Val
|
|
NM_024915.4:c.170A>T
MANE Select
|
NP_079191.2:p.Asp57Val
|
|