ENST00000477226.6:n.717C>T
|
|
|
ENST00000683013.1:n.631C>T
|
|
|
ENST00000373960.4:c.1243C>T
MANE Select
|
ENSP00000363071.3:p.Arg415Trp
|
|
ENST00000373960.3:c.1243C>T
|
ENSP00000363071.3:p.Arg415Trp
|
|
ENST00000477226.5:n.715C>T
|
|
|
ENST00000492726.1:n.638C>T
|
|
|
NM_001927.3:c.1243C>T , LRG_380t1:c.1243C>T
|
NP_001918.3:p.Arg415Trp
|
|
NM_001927.4:c.1243C>T
MANE Select
|
NP_001918.3:p.Arg415Trp
|
|
NM_001382708.1:c.1240C>T
|
NP_001369637.1:p.Arg414Trp
|
|
NM_001382709.1:c.811C>T
|
NP_001369638.1:p.Arg271Trp
|
|
NM_001382710.1:c.1174C>T
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NP_001369639.1:p.Arg392Trp
|
|
NM_001382711.1:c.1222C>T
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NP_001369640.1:p.Arg408Trp
|
|
NM_001382712.1:c.1243C>T
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NP_001369641.1:p.Arg415Trp
|
|
NM_001382713.1:c.973C>T
|
NP_001369642.1:p.Arg325Trp
|
|