ENST00000691183.1:c.*260G>T
|
ENSP00000509954.1:n.*260G>T
|
|
ENST00000378842.8:c.672G>T
MANE Select
|
ENSP00000368119.4:p.Gln224His
|
|
ENST00000378842.7:c.672G>T
|
ENSP00000368119.3:p.Gln224His
|
|
ENST00000450095.6:c.345G>T
|
ENSP00000401956.2:p.Gln115His
|
|
ENST00000472111.5:n.928G>T
|
|
|
ENST00000473506.6:c.*260G>T
|
ENSP00000432839.2:n.*260G>T
|
|
ENST00000473529.5:n.831G>T
|
|
|
ENST00000487381.5:n.1057G>T
|
|
|
ENST00000489643.6:n.447G>T
|
|
|
ENST00000554085.5:c.*416G>T
|
ENSP00000450419.1:n.*416G>T
|
|
ENST00000554550.5:c.*292G>T
|
ENSP00000451435.1:n.*292G>T
|
|
ENST00000554638.5:n.1144G>T
|
|
|
ENST00000555020.5:n.828G>T
|
|
|
ENST00000555086.5:n.676G>T
|
|
|
ENST00000555214.5:n.493G>T
|
|
|
ENST00000555754.1:n.17G>T
|
|
|
ENST00000556244.1:c.659G>T
|
|
|
ENST00000556278.1:c.417G>T
|
ENSP00000451792.1:p.Gln139His
|
|
ENST00000556494.5:n.793G>T
|
|
|
ENST00000557706.5:n.1234G>T
|
|
|
NM_000155.3:c.672G>T
|
NP_000146.2:p.Gln224His
|
|
NM_001258332.1:c.345G>T
|
NP_001245261.1:p.Gln115His
|
|
NM_000155.4:c.672G>T
MANE Select
|
NP_000146.2:p.Gln224His
|
|
NM_001258332.2:c.345G>T
|
NP_001245261.1:p.Gln115His
|
|