ENST00000342245.9:c.1587G>C
MANE Select
|
ENSP00000340409.4:p.Pro529=
|
|
ENST00000342245.8:c.1587G>C
|
ENSP00000340409.4:p.Pro529=
|
|
ENST00000526280.1:c.644G>C
|
|
|
ENST00000527275.5:c.1584G>C
|
ENSP00000435350.1:p.Pro528=
|
|
ENST00000531303.5:c.*438G>C
|
ENSP00000432625.1:n.*438G>C
|
|
ENST00000531336.1:n.575G>C
|
|
|
ENST00000533123.5:c.*314G>C
|
ENSP00000435950.1:n.*314G>C
|
|
ENST00000534405.5:c.*418G>C
|
ENSP00000434353.1:n.*418G>C
|
|
NM_000543.4:c.1587G>C
|
NP_000534.3:p.Pro529=
|
|
NM_001007593.2:c.1584G>C
|
NP_001007594.2:p.Pro528=
|
|
XM_005253075.3:c.*80G>C
|
XP_005253132.1:n.*80G>C
|
|
XM_011520303.1:c.1455G>C
|
XP_011518605.1:p.Pro485=
|
|
XM_011520304.1:c.*80G>C
|
XP_011518606.1:n.*80G>C
|
|
NM_001318087.1:c.*80G>C
|
NP_001305016.1:n.*80G>C
|
|
NM_001318088.1:c.666G>C
|
NP_001305017.1:p.Pro222=
|
|
NM_001365135.1:c.1455G>C
|
NP_001352064.1:p.Pro485=
|
|
NR_027400.2:n.1600G>C
|
|
|
NR_134502.1:n.1139G>C
|
|
|
XM_011520304.2:c.*80G>C
|
XP_011518606.1:n.*80G>C
|
|
XR_001747940.2:n.1772G>C
|
|
|
XR_002957158.1:n.1954G>C
|
|
|
NM_000543.5:c.1587G>C
MANE Select
|
NP_000534.3:p.Pro529=
|
|
NM_001007593.3:c.1584G>C
|
NP_001007594.2:p.Pro528=
|
|
NM_001318087.2:c.*80G>C
|
NP_001305016.1:n.*80G>C
|
|
NM_001318088.2:c.666G>C
|
NP_001305017.1:p.Pro222=
|
|
NM_001365135.2:c.1455G>C
|
NP_001352064.1:p.Pro485=
|
|
NR_027400.3:n.1540G>C
|
|
|
NR_134502.2:n.1079G>C
|
|
|