ENST00000348974.5:c.759T>G
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ENSP00000330021.7:p.Ala253=
|
|
ENST00000394236.9:c.759T>G
MANE Select
|
ENSP00000377783.3:p.Ala253=
|
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ENST00000407433.6:c.714T>G
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ENSP00000385794.2:p.Ala238=
|
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ENST00000647936.1:c.759T>G
|
ENSP00000496822.1:p.Ala253=
|
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ENST00000648381.1:n.927T>G
|
|
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ENST00000648853.1:c.717T>G
|
ENSP00000497262.1:p.Ala239=
|
|
ENST00000649103.1:c.858T>G
|
ENSP00000497962.1:n.858T>G
|
|
ENST00000650591.1:c.855T>G
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ENSP00000497376.1:p.Ala285=
|
|
ENST00000394236.7:c.759T>G
|
ENSP00000377783.3:p.Ala253=
|
|
ENST00000407433.5:c.366T>G
|
ENSP00000385794.1:p.Ala122=
|
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NM_000313.3:c.759T>G , LRG_572t1:c.759T>G
|
NP_000304.2:p.Ala253=
|
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NM_001314077.1:c.855T>G , LRG_572t2:c.855T>G
|
NP_001301006.1:p.Ala285=
|
|
NM_000313.4:c.759T>G
MANE Select
|
NP_000304.2:p.Ala253=
|
|
NM_001314077.2:c.855T>G
|
NP_001301006.1:p.Ala285=
|
|