ENST00000691183.1:c.*209G>C
|
ENSP00000509954.1:n.*209G>C
|
|
ENST00000378842.8:c.621G>C
MANE Select
|
ENSP00000368119.4:p.Gln207His
|
|
ENST00000378842.7:c.621G>C
|
ENSP00000368119.3:p.Gln207His
|
|
ENST00000450095.6:c.294G>C
|
ENSP00000401956.2:p.Gln98His
|
|
ENST00000472111.5:n.877G>C
|
|
|
ENST00000473506.6:c.*209G>C
|
ENSP00000432839.2:n.*209G>C
|
|
ENST00000473529.5:n.780G>C
|
|
|
ENST00000487381.5:n.1006G>C
|
|
|
ENST00000489643.6:n.396G>C
|
|
|
ENST00000554085.5:c.*365G>C
|
ENSP00000450419.1:n.*365G>C
|
|
ENST00000554550.5:c.*241G>C
|
ENSP00000451435.1:n.*241G>C
|
|
ENST00000554638.5:n.1093G>C
|
|
|
ENST00000555020.5:n.777G>C
|
|
|
ENST00000555086.5:n.625G>C
|
|
|
ENST00000555214.5:n.442G>C
|
|
|
ENST00000556244.1:c.608G>C
|
|
|
ENST00000556278.1:c.366G>C
|
ENSP00000451792.1:p.Gln122His
|
|
ENST00000556494.5:n.742G>C
|
|
|
ENST00000557706.5:n.1183G>C
|
|
|
NM_000155.3:c.621G>C
|
NP_000146.2:p.Gln207His
|
|
NM_001258332.1:c.294G>C
|
NP_001245261.1:p.Gln98His
|
|
NM_000155.4:c.621G>C
MANE Select
|
NP_000146.2:p.Gln207His
|
|
NM_001258332.2:c.294G>C
|
NP_001245261.1:p.Gln98His
|
|