ENST00000355832.10:c.3805G>A
MANE Select
|
ENSP00000348089.5:p.Asp1269Asn
|
|
ENST00000679552.1:n.876G>A
|
|
|
ENST00000679871.1:n.951G>A
|
|
|
ENST00000679974.1:n.854G>A
|
|
|
ENST00000681632.1:n.5208G>A
|
|
|
ENST00000681659.1:c.3646G>A
|
ENSP00000505631.1:p.Asp1216Asn
|
|
ENST00000355832.9:c.3805G>A
|
ENSP00000348089.5:p.Asp1269Asn
|
|
ENST00000465653.1:n.127G>A
|
|
|
ENST00000623073.3:c.*2101G>A
|
ENSP00000485650.1:n.*2101G>A
|
|
ENST00000623115.3:c.1915G>A
|
ENSP00000485321.1:p.Asp639Asn
|
|
ENST00000624341.3:c.1637G>A
|
|
|
NM_000124.3:c.3805G>A
|
NP_000115.1:p.Asp1269Asn
|
|
XR_945953.1:n.243-10035C>T
|
|
|
NM_001346440.1:c.3805G>A
|
NP_001333369.1:p.Asp1269Asn
|
|
NM_000124.4:c.3805G>A
MANE Select
|
NP_000115.1:p.Asp1269Asn
|
|
NM_001346440.2:c.3805G>A
|
NP_001333369.1:p.Asp1269Asn
|
|