ENST00000375448.4:c.1358C>T
MANE Select
|
ENSP00000364597.4:p.Ala453Val
|
|
ENST00000467001.1:n.259C>T
|
|
|
ENST00000487048.5:n.325C>T
|
|
|
NM_012387.2:c.1358C>T
|
NP_036519.2:p.Ala453Val
|
|
XM_011541150.1:c.1172C>T
|
XP_011539452.1:p.Ala391Val
|
|
XM_011541151.1:c.1156-327C>T
|
XP_011539453.1:n.1156-327C>T
|
|
XM_011541152.1:c.821C>T
|
XP_011539454.1:p.Ala274Val
|
|
XM_011541154.1:c.*95C>T
|
XP_011539456.1:n.*95C>T
|
|
XM_011541156.1:c.*42C>T
|
XP_011539458.1:n.*42C>T
|
|
XM_011541157.1:c.467C>T
|
XP_011539459.1:p.Ala156Val
|
|
XM_011541154.2:c.*95C>T
|
XP_011539456.1:n.*95C>T
|
|
NM_012387.3:c.1358C>T
MANE Select
|
NP_036519.2:p.Ala453Val
|
|