ENST00000477226.6:n.650C=
|
|
|
ENST00000683013.1:n.564C=
|
|
|
ENST00000373960.4:c.1176C=
MANE Select
|
ENSP00000363071.3:p.Leu392=
|
|
ENST00000373960.3:c.1176C=
|
ENSP00000363071.3:p.Leu392=
|
|
ENST00000477226.5:n.648C=
|
|
|
ENST00000492726.1:n.571C=
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|
|
NM_001927.3:c.1176C= , LRG_380t1:c.1176C=
|
NP_001918.3:p.Leu392=
|
|
NM_001927.4:c.1176C=
MANE Select
|
NP_001918.3:p.Leu392=
|
|
NM_001382708.1:c.1173C=
|
NP_001369637.1:p.Leu391=
|
|
NM_001382709.1:c.744C=
|
NP_001369638.1:p.Leu248=
|
|
NM_001382710.1:c.1107C=
|
NP_001369639.1:p.Leu369=
|
|
NM_001382711.1:c.1155C=
|
NP_001369640.1:p.Leu385=
|
|
NM_001382712.1:c.1176C=
|
NP_001369641.1:p.Leu392=
|
|
NM_001382713.1:c.906C=
|
NP_001369642.1:p.Leu302=
|
|