ENST00000477226.6:n.698G>C
|
|
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ENST00000683013.1:n.612G>C
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|
|
ENST00000373960.4:c.1224G>C
MANE Select
|
ENSP00000363071.3:p.Leu408=
|
|
ENST00000373960.3:c.1224G>C
|
ENSP00000363071.3:p.Leu408=
|
|
ENST00000477226.5:n.696G>C
|
|
|
ENST00000492726.1:n.619G>C
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|
|
NM_001927.3:c.1224G>C , LRG_380t1:c.1224G>C
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NP_001918.3:p.Leu408=
|
|
NM_001927.4:c.1224G>C
MANE Select
|
NP_001918.3:p.Leu408=
|
|
NM_001382708.1:c.1221G>C
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NP_001369637.1:p.Leu407=
|
|
NM_001382709.1:c.792G>C
|
NP_001369638.1:p.Leu264=
|
|
NM_001382710.1:c.1155G>C
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NP_001369639.1:p.Leu385=
|
|
NM_001382711.1:c.1203G>C
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NP_001369640.1:p.Leu401=
|
|
NM_001382712.1:c.1224G>C
|
NP_001369641.1:p.Leu408=
|
|
NM_001382713.1:c.954G>C
|
NP_001369642.1:p.Leu318=
|
|