ENST00000355832.10:c.1548G>T
MANE Select
|
ENSP00000348089.5:p.Arg516Ser
|
|
ENST00000681632.1:n.1626G>T
|
|
|
ENST00000681659.1:c.1526+5209G>T
|
ENSP00000505631.1:n.1526+5209G>T
|
|
ENST00000355832.9:c.1548G>T
|
ENSP00000348089.5:p.Arg516Ser
|
|
ENST00000475116.1:n.138G>T
|
|
|
ENST00000623073.3:c.-52G>T
|
ENSP00000485650.1:n.-52G>T
|
|
ENST00000623115.3:c.-207G>T
|
ENSP00000485321.1:n.-207G>T
|
|
ENST00000623318.1:c.-52G>T
|
ENSP00000485423.1:n.-52G>T
|
|
ENST00000623788.1:n.547G>T
|
|
|
NM_000124.3:c.1548G>T
|
NP_000115.1:p.Arg516Ser
|
|
NM_001346440.1:c.1548G>T
|
NP_001333369.1:p.Arg516Ser
|
|
NM_000124.4:c.1548G>T
MANE Select
|
NP_000115.1:p.Arg516Ser
|
|
NM_001346440.2:c.1548G>T
|
NP_001333369.1:p.Arg516Ser
|
|