ENST00000355832.10:c.3095C>A
MANE Select
|
ENSP00000348089.5:p.Pro1032His
|
|
ENST00000679552.1:n.166C>A
|
|
|
ENST00000679871.1:n.241C>A
|
|
|
ENST00000679974.1:n.144C>A
|
|
|
ENST00000681632.1:n.4498C>A
|
|
|
ENST00000681659.1:c.2936C>A
|
ENSP00000505631.1:p.Pro979His
|
|
ENST00000355832.9:c.3095C>A
|
ENSP00000348089.5:p.Pro1032His
|
|
ENST00000623073.3:c.*1391C>A
|
ENSP00000485650.1:n.*1391C>A
|
|
ENST00000623115.3:c.1205C>A
|
ENSP00000485321.1:p.Pro402His
|
|
ENST00000624341.3:c.927C>A
|
|
|
NM_000124.3:c.3095C>A
|
NP_000115.1:p.Pro1032His
|
|
XR_945953.1:n.243-700G>T
|
|
|
NM_001346440.1:c.3095C>A
|
NP_001333369.1:p.Pro1032His
|
|
NM_000124.4:c.3095C>A
MANE Select
|
NP_000115.1:p.Pro1032His
|
|
NM_001346440.2:c.3095C>A
|
NP_001333369.1:p.Pro1032His
|
|