ENST00000695850.1:n.1365C>G
|
|
|
ENST00000695852.1:n.296C>G
|
|
|
ENST00000695853.1:c.*1248C>G
|
ENSP00000512218.1:n.*1248C>G
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|
ENST00000423902.7:c.8189C>G
MANE Select
|
ENSP00000392028.1:p.Ala2730Gly
|
|
ENST00000423902.6:c.8189C>G
|
ENSP00000392028.1:p.Ala2730Gly
|
|
ENST00000524602.5:c.2042C>G
|
ENSP00000437061.1:p.Ala681Gly
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|
ENST00000528280.1:n.235C>G
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|
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ENST00000532149.1:n.611C>G
|
|
|
NM_001316690.1:c.2042C>G
|
NP_001303619.1:p.Ala681Gly
|
|
NM_017780.3:c.8189C>G
|
NP_060250.2:p.Ala2730Gly
|
|
XM_011517553.1:c.8279C>G
|
XP_011515855.1:p.Ala2760Gly
|
|
XM_011517554.1:c.8279C>G
|
XP_011515856.1:p.Ala2760Gly
|
|
XM_011517555.1:c.8276C>G
|
XP_011515857.1:p.Ala2759Gly
|
|
XM_011517556.1:c.8057C>G
|
XP_011515858.1:p.Ala2686Gly
|
|
XM_011517557.1:c.6266C>G
|
XP_011515859.1:p.Ala2089Gly
|
|
XM_011517558.1:c.5816C>G
|
XP_011515860.1:p.Ala1939Gly
|
|
XM_011517559.1:c.5024C>G
|
XP_011515861.1:p.Ala1675Gly
|
|
XM_011517553.2:c.8279C>G
|
XP_011515855.1:p.Ala2760Gly
|
|
XM_011517554.3:c.8279C>G
|
XP_011515856.1:p.Ala2760Gly
|
|
XM_011517555.2:c.8276C>G
|
XP_011515857.1:p.Ala2759Gly
|
|
XM_017013612.1:c.8279C>G
|
XP_016869101.1:p.Ala2760Gly
|
|
XM_017013613.1:c.8186C>G
|
XP_016869102.1:p.Ala2729Gly
|
|
NM_017780.4:c.8189C>G
MANE Select
|
NP_060250.2:p.Ala2730Gly
|
|