ENST00000375448.4:c.1360C>T
MANE Select
|
ENSP00000364597.4:p.Gln454Ter
|
|
ENST00000467001.1:n.261C>T
|
|
|
ENST00000487048.5:n.327C>T
|
|
|
NM_012387.2:c.1360C>T
|
NP_036519.2:p.Gln454Ter
|
|
XM_011541150.1:c.1174C>T
|
XP_011539452.1:p.Gln392Ter
|
|
XM_011541151.1:c.1156-325C>T
|
XP_011539453.1:n.1156-325C>T
|
|
XM_011541152.1:c.823C>T
|
XP_011539454.1:p.Gln275Ter
|
|
XM_011541154.1:c.*97C>T
|
XP_011539456.1:n.*97C>T
|
|
XM_011541156.1:c.*44C>T
|
XP_011539458.1:n.*44C>T
|
|
XM_011541157.1:c.469C>T
|
XP_011539459.1:p.Gln157Ter
|
|
XM_011541154.2:c.*97C>T
|
XP_011539456.1:n.*97C>T
|
|
NM_012387.3:c.1360C>T
MANE Select
|
NP_036519.2:p.Gln454Ter
|
|