ENST00000695850.1:n.1665C>G
|
|
|
ENST00000695852.1:n.596C>G
|
|
|
ENST00000695853.1:c.*1548C>G
|
ENSP00000512218.1:n.*1548C>G
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|
ENST00000423902.7:c.8489C>G
MANE Select
|
ENSP00000392028.1:p.Ala2830Gly
|
|
ENST00000423902.6:c.8489C>G
|
ENSP00000392028.1:p.Ala2830Gly
|
|
ENST00000524602.5:c.2342C>G
|
ENSP00000437061.1:p.Ala781Gly
|
|
ENST00000528280.1:n.535C>G
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|
|
NM_001316690.1:c.2342C>G
|
NP_001303619.1:p.Ala781Gly
|
|
NM_017780.3:c.8489C>G
|
NP_060250.2:p.Ala2830Gly
|
|
XM_011517553.1:c.8579C>G
|
XP_011515855.1:p.Ala2860Gly
|
|
XM_011517554.1:c.8579C>G
|
XP_011515856.1:p.Ala2860Gly
|
|
XM_011517555.1:c.8576C>G
|
XP_011515857.1:p.Ala2859Gly
|
|
XM_011517556.1:c.8357C>G
|
XP_011515858.1:p.Ala2786Gly
|
|
XM_011517557.1:c.6566C>G
|
XP_011515859.1:p.Ala2189Gly
|
|
XM_011517558.1:c.6116C>G
|
XP_011515860.1:p.Ala2039Gly
|
|
XM_011517559.1:c.5324C>G
|
XP_011515861.1:p.Ala1775Gly
|
|
XM_011517553.2:c.8579C>G
|
XP_011515855.1:p.Ala2860Gly
|
|
XM_011517554.3:c.8579C>G
|
XP_011515856.1:p.Ala2860Gly
|
|
XM_011517555.2:c.8576C>G
|
XP_011515857.1:p.Ala2859Gly
|
|
XM_017013612.1:c.8579C>G
|
XP_016869101.1:p.Ala2860Gly
|
|
XM_017013613.1:c.8486C>G
|
XP_016869102.1:p.Ala2829Gly
|
|
NM_017780.4:c.8489C>G
MANE Select
|
NP_060250.2:p.Ala2830Gly
|
|