ENST00000262461.7:c.3559T>C
MANE Select
|
ENSP00000262461.2:p.Leu1187=
|
|
ENST00000262461.6:c.3559T>C
|
ENSP00000262461.2:p.Leu1187=
|
|
ENST00000343225.4:c.3511T>C
|
ENSP00000340878.4:p.Leu1171=
|
|
ENST00000509205.5:c.*172T>C
|
ENSP00000427109.1:n.*172T>C
|
|
NM_001046.2:c.3559T>C
|
NP_001037.1:p.Leu1187=
|
|
NM_001256461.1:c.3511T>C
|
NP_001243390.1:p.Leu1171=
|
|
NR_046207.1:n.3789T>C
|
|
|
XM_017009771.1:c.1801T>C
|
XP_016865260.1:p.Leu601=
|
|
XR_001742214.1:n.3783T>C
|
|
|
NM_001046.3:c.3559T>C
MANE Select
|
NP_001037.1:p.Leu1187=
|
|
NM_001256461.2:c.3511T>C
|
NP_001243390.1:p.Leu1171=
|
|
NR_046207.2:n.3814T>C
|
|
|