|
ENST00000691183.1:c.*268T>C
|
ENSP00000509954.1:n.*268T>C
|
|
|
ENST00000378842.8:c.680T>C
MANE Select
|
ENSP00000368119.4:p.Leu227Pro
|
|
|
ENST00000378842.7:c.680T>C
|
ENSP00000368119.3:p.Leu227Pro
|
|
|
ENST00000450095.6:c.353T>C
|
ENSP00000401956.2:p.Leu118Pro
|
|
|
ENST00000472111.5:n.936T>C
|
|
|
|
ENST00000473506.6:c.*268T>C
|
ENSP00000432839.2:n.*268T>C
|
|
|
ENST00000473529.5:n.839T>C
|
|
|
|
ENST00000487381.5:n.1065T>C
|
|
|
|
ENST00000489643.6:n.455T>C
|
|
|
|
ENST00000554085.5:c.*424T>C
|
ENSP00000450419.1:n.*424T>C
|
|
|
ENST00000554550.5:c.*300T>C
|
ENSP00000451435.1:n.*300T>C
|
|
|
ENST00000554638.5:n.1152T>C
|
|
|
|
ENST00000555020.5:n.836T>C
|
|
|
|
ENST00000555086.5:n.684T>C
|
|
|
|
ENST00000555214.5:n.501T>C
|
|
|
|
ENST00000555754.1:n.25T>C
|
|
|
|
ENST00000556244.1:c.667T>C
|
|
|
|
ENST00000556278.1:c.425T>C
|
ENSP00000451792.1:p.Leu142Pro
|
|
|
ENST00000556494.5:n.801T>C
|
|
|
|
ENST00000557706.5:n.1242T>C
|
|
|
|
NM_000155.3:c.680T>C
|
NP_000146.2:p.Leu227Pro
|
|
|
NM_001258332.1:c.353T>C
|
NP_001245261.1:p.Leu118Pro
|
|
|
NM_000155.4:c.680T>C
MANE Select
|
NP_000146.2:p.Leu227Pro
|
|
|
NM_001258332.2:c.353T>C
|
NP_001245261.1:p.Leu118Pro
|
|
