ENST00000420175.3:c.44A>T
MANE Select
|
ENSP00000391137.2:p.Glu15Val
|
|
ENST00000275838.5:c.44A>T
|
ENSP00000275838.1:p.Glu15Val
|
|
ENST00000377867.7:c.271+365A>T
|
ENSP00000367098.3:n.271+365A>T
|
|
ENST00000415615.1:c.*122-34A>T
|
ENSP00000410871.1:n.*122-34A>T
|
|
ENST00000420175.2:c.44A>T
|
ENSP00000391137.2:p.Glu15Val
|
|
NM_001142459.1:c.44A>T
|
NP_001135931.2:p.Glu15Val
|
|
NM_001142460.1:c.44A>T
|
NP_001135932.2:p.Glu15Val
|
|
NM_080871.3:c.271+365A>T
|
NP_543147.2:n.271+365A>T
|
|
XM_005249949.3:c.179A>T
|
XP_005250006.1:p.Glu60Val
|
|
NM_001142459.2:c.44A>T
MANE Select
|
NP_001135931.2:p.Glu15Val
|
|
NM_080871.4:c.271+365A>T
|
NP_543147.2:n.271+365A>T
|
|