ENST00000354638.8:c.2327C>G
MANE Select
|
ENSP00000346659.3:p.Ala776Gly
|
|
ENST00000353809.9:c.2255C>G
|
ENSP00000261276.8:p.Ala752Gly
|
|
ENST00000354638.7:c.2327C>G
|
ENSP00000346659.3:p.Ala776Gly
|
|
NM_000275.2:c.2327C>G
|
NP_000266.2:p.Ala776Gly
|
|
NM_001300984.1:c.2255C>G
|
NP_001287913.1:p.Ala752Gly
|
|
XM_011521639.1:c.2393C>G
|
XP_011519941.1:p.Ala798Gly
|
|
XM_011521640.1:c.2369C>G
|
XP_011519942.1:p.Ala790Gly
|
|
XM_011521641.1:c.2351C>G
|
XP_011519943.1:p.Ala784Gly
|
|
XM_011521642.1:c.2321C>G
|
XP_011519944.1:p.Ala774Gly
|
|
XM_011521643.1:c.2279C>G
|
XP_011519945.1:p.Ala760Gly
|
|
XM_011521644.1:c.2255C>G
|
XP_011519946.1:p.Ala752Gly
|
|
XM_011521645.1:c.2186C>G
|
XP_011519947.1:p.Ala729Gly
|
|
XM_011521640.2:c.2369C>G
|
XP_011519942.1:p.Ala790Gly
|
|
XM_017022255.1:c.2393C>G
|
XP_016877744.1:p.Ala798Gly
|
|
XM_017022256.1:c.2351C>G
|
XP_016877745.1:p.Ala784Gly
|
|
XM_017022257.1:c.2321C>G
|
XP_016877746.1:p.Ala774Gly
|
|
XM_017022258.1:c.2351C>G
|
XP_016877747.1:p.Ala784Gly
|
|
XM_017022259.1:c.2279C>G
|
XP_016877748.1:p.Ala760Gly
|
|
XM_017022260.1:c.2255C>G
|
XP_016877749.1:p.Ala752Gly
|
|
XM_017022261.1:c.2198C>G
|
XP_016877750.1:p.Ala733Gly
|
|
XM_017022262.1:c.2268+19761C>G
|
XP_016877751.1:n.2268+19761C>G
|
|
XM_017022263.1:c.2186C>G
|
XP_016877752.1:p.Ala729Gly
|
|
XM_017022264.1:c.2186C>G
|
XP_016877753.1:p.Ala729Gly
|
|
NM_000275.3:c.2327C>G
MANE Select
|
NP_000266.2:p.Ala776Gly
|
|
NM_001300984.2:c.2255C>G
|
NP_001287913.1:p.Ala752Gly
|
|