ENST00000261769.10:c.2077G>C
MANE Select
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ENSP00000261769.4:p.Gly693Arg
|
|
ENST00000261769.9:c.2077G>C
|
ENSP00000261769.4:p.Gly693Arg
|
|
ENST00000422392.6:c.1894G>C
|
ENSP00000414946.2:p.Gly632Arg
|
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ENST00000562118.1:n.295G>C
|
|
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ENST00000562836.5:n.2148G>C
|
|
|
ENST00000566510.5:c.*743G>C
|
ENSP00000458139.1:n.*743G>C
|
|
ENST00000566612.5:c.*317G>C
|
ENSP00000454782.1:n.*317G>C
|
|
ENST00000611625.4:c.2140G>C
|
ENSP00000481063.1:p.Gly714Arg
|
|
ENST00000612417.4:c.1830+1420G>C
|
ENSP00000478360.1:n.1830+1420G>C
|
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ENST00000621016.4:c.1865+1385G>C
|
ENSP00000480664.1:n.1865+1385G>C
|
|
NM_004360.3:c.2077G>C , LRG_301t1:c.2077G>C
|
NP_004351.1:p.Gly693Arg
|
|
XM_011523488.1:c.1342G>C
|
XP_011521790.1:p.Gly448Arg
|
|
XM_011523489.1:c.1342G>C
|
XP_011521791.1:p.Gly448Arg
|
|
NM_001317184.1:c.1894G>C
|
NP_001304113.1:p.Gly632Arg
|
|
NM_001317185.1:c.529G>C
|
NP_001304114.1:p.Gly177Arg
|
|
NM_001317186.1:c.112G>C
|
NP_001304115.1:p.Gly38Arg
|
|
NM_004360.4:c.2077G>C
|
NP_004351.1:p.Gly693Arg
|
|
NM_004360.5:c.2077G>C
MANE Select
|
NP_004351.1:p.Gly693Arg
|
|
NM_001317184.2:c.1894G>C
|
NP_001304113.1:p.Gly632Arg
|
|
NM_001317185.2:c.529G>C
|
NP_001304114.1:p.Gly177Arg
|
|
NM_001317186.2:c.112G>C
|
NP_001304115.1:p.Gly38Arg
|
|