ENST00000691183.1:c.*352T>C
|
ENSP00000509954.1:n.*352T>C
|
|
ENST00000378842.8:c.764T>C
MANE Select
|
ENSP00000368119.4:p.Leu255Pro
|
|
ENST00000378842.7:c.764T>C
|
ENSP00000368119.3:p.Leu255Pro
|
|
ENST00000450095.6:c.437T>C
|
ENSP00000401956.2:p.Leu146Pro
|
|
ENST00000473506.6:c.*352T>C
|
ENSP00000432839.2:n.*352T>C
|
|
ENST00000489643.6:n.844T>C
|
|
|
ENST00000554085.5:c.*508T>C
|
ENSP00000450419.1:n.*508T>C
|
|
ENST00000554550.5:c.*384T>C
|
ENSP00000451435.1:n.*384T>C
|
|
ENST00000554638.5:n.1236T>C
|
|
|
ENST00000555020.5:n.1225T>C
|
|
|
ENST00000555086.5:n.768T>C
|
|
|
ENST00000555754.1:n.109T>C
|
|
|
ENST00000556244.1:c.751T>C
|
|
|
ENST00000556278.1:c.432+382T>C
|
ENSP00000451792.1:n.432+382T>C
|
|
ENST00000557706.5:n.1326T>C
|
|
|
NM_000155.3:c.764T>C
|
NP_000146.2:p.Leu255Pro
|
|
NM_001258332.1:c.437T>C
|
NP_001245261.1:p.Leu146Pro
|
|
NM_000155.4:c.764T>C
MANE Select
|
NP_000146.2:p.Leu255Pro
|
|
NM_001258332.2:c.437T>C
|
NP_001245261.1:p.Leu146Pro
|
|