ENST00000695850.1:n.1591C>G
|
|
|
ENST00000695852.1:n.522C>G
|
|
|
ENST00000695853.1:c.*1474C>G
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ENSP00000512218.1:n.*1474C>G
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|
ENST00000423902.7:c.8415C>G
MANE Select
|
ENSP00000392028.1:p.Gly2805=
|
|
ENST00000423902.6:c.8415C>G
|
ENSP00000392028.1:p.Gly2805=
|
|
ENST00000524602.5:c.2268C>G
|
ENSP00000437061.1:p.Gly756=
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|
ENST00000528280.1:n.461C>G
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|
|
NM_001316690.1:c.2268C>G
|
NP_001303619.1:p.Gly756=
|
|
NM_017780.3:c.8415C>G
|
NP_060250.2:p.Gly2805=
|
|
XM_011517553.1:c.8505C>G
|
XP_011515855.1:p.Gly2835=
|
|
XM_011517554.1:c.8505C>G
|
XP_011515856.1:p.Gly2835=
|
|
XM_011517555.1:c.8502C>G
|
XP_011515857.1:p.Gly2834=
|
|
XM_011517556.1:c.8283C>G
|
XP_011515858.1:p.Gly2761=
|
|
XM_011517557.1:c.6492C>G
|
XP_011515859.1:p.Gly2164=
|
|
XM_011517558.1:c.6042C>G
|
XP_011515860.1:p.Gly2014=
|
|
XM_011517559.1:c.5250C>G
|
XP_011515861.1:p.Gly1750=
|
|
XM_011517553.2:c.8505C>G
|
XP_011515855.1:p.Gly2835=
|
|
XM_011517554.3:c.8505C>G
|
XP_011515856.1:p.Gly2835=
|
|
XM_011517555.2:c.8502C>G
|
XP_011515857.1:p.Gly2834=
|
|
XM_017013612.1:c.8505C>G
|
XP_016869101.1:p.Gly2835=
|
|
XM_017013613.1:c.8412C>G
|
XP_016869102.1:p.Gly2804=
|
|
NM_017780.4:c.8415C>G
MANE Select
|
NP_060250.2:p.Gly2805=
|
|