ENST00000355832.10:c.3874G>C
MANE Select
|
ENSP00000348089.5:p.Asp1292His
|
|
ENST00000679552.1:n.945G>C
|
|
|
ENST00000679871.1:n.1020G>C
|
|
|
ENST00000679974.1:n.923G>C
|
|
|
ENST00000681632.1:n.5277G>C
|
|
|
ENST00000681659.1:c.3715G>C
|
ENSP00000505631.1:p.Asp1239His
|
|
ENST00000355832.9:c.3874G>C
|
ENSP00000348089.5:p.Asp1292His
|
|
ENST00000465653.1:n.196G>C
|
|
|
ENST00000623073.3:c.*2170G>C
|
ENSP00000485650.1:n.*2170G>C
|
|
ENST00000623115.3:c.1984G>C
|
ENSP00000485321.1:p.Asp662His
|
|
ENST00000624341.3:c.1706G>C
|
|
|
NM_000124.3:c.3874G>C
|
NP_000115.1:p.Asp1292His
|
|
XR_945953.1:n.243-10104C>G
|
|
|
NM_001346440.1:c.3874G>C
|
NP_001333369.1:p.Asp1292His
|
|
NM_000124.4:c.3874G>C
MANE Select
|
NP_000115.1:p.Asp1292His
|
|
NM_001346440.2:c.3874G>C
|
NP_001333369.1:p.Asp1292His
|
|