ENST00000354638.8:c.2311G>T
MANE Select
|
ENSP00000346659.3:p.Ala771Ser
|
|
ENST00000353809.9:c.2239G>T
|
ENSP00000261276.8:p.Ala747Ser
|
|
ENST00000354638.7:c.2311G>T
|
ENSP00000346659.3:p.Ala771Ser
|
|
NM_000275.2:c.2311G>T
|
NP_000266.2:p.Ala771Ser
|
|
NM_001300984.1:c.2239G>T
|
NP_001287913.1:p.Ala747Ser
|
|
XM_011521639.1:c.2377G>T
|
XP_011519941.1:p.Ala793Ser
|
|
XM_011521640.1:c.2353G>T
|
XP_011519942.1:p.Ala785Ser
|
|
XM_011521641.1:c.2335G>T
|
XP_011519943.1:p.Ala779Ser
|
|
XM_011521642.1:c.2305G>T
|
XP_011519944.1:p.Ala769Ser
|
|
XM_011521643.1:c.2263G>T
|
XP_011519945.1:p.Ala755Ser
|
|
XM_011521644.1:c.2239G>T
|
XP_011519946.1:p.Ala747Ser
|
|
XM_011521645.1:c.2170G>T
|
XP_011519947.1:p.Ala724Ser
|
|
XM_011521640.2:c.2353G>T
|
XP_011519942.1:p.Ala785Ser
|
|
XM_017022255.1:c.2377G>T
|
XP_016877744.1:p.Ala793Ser
|
|
XM_017022256.1:c.2335G>T
|
XP_016877745.1:p.Ala779Ser
|
|
XM_017022257.1:c.2305G>T
|
XP_016877746.1:p.Ala769Ser
|
|
XM_017022258.1:c.2335G>T
|
XP_016877747.1:p.Ala779Ser
|
|
XM_017022259.1:c.2263G>T
|
XP_016877748.1:p.Ala755Ser
|
|
XM_017022260.1:c.2239G>T
|
XP_016877749.1:p.Ala747Ser
|
|
XM_017022261.1:c.2182G>T
|
XP_016877750.1:p.Ala728Ser
|
|
XM_017022262.1:c.2268+19745G>T
|
XP_016877751.1:n.2268+19745G>T
|
|
XM_017022263.1:c.2170G>T
|
XP_016877752.1:p.Ala724Ser
|
|
XM_017022264.1:c.2170G>T
|
XP_016877753.1:p.Ala724Ser
|
|
NM_000275.3:c.2311G>T
MANE Select
|
NP_000266.2:p.Ala771Ser
|
|
NM_001300984.2:c.2239G>T
|
NP_001287913.1:p.Ala747Ser
|
|