ENST00000311907.10:c.642C=
MANE Select
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ENSP00000308541.5:p.Val214=
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ENST00000311907.9:c.642C=
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ENSP00000308541.5:p.Val214=
|
|
ENST00000442468.1:c.612C=
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ENSP00000387413.1:p.Val204=
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ENST00000490274.1:n.422C=
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|
|
ENST00000530231.5:c.642C=
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ENSP00000433907.1:p.Val214=
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NM_000506.3:c.642C=
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NP_000497.1:p.Val214=
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NM_000506.4:c.642C= , LRG_551t1:c.642C=
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NP_000497.1:p.Val214=
|
|
NM_001311257.1:c.594C=
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NP_001298186.1:p.Val198=
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XR_428840.2:n.686C=
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|
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XR_428840.4:n.677C=
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|
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NM_000506.5:c.642C=
MANE Select
|
NP_000497.1:p.Val214=
|
|
NM_001311257.2:c.594C=
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NP_001298186.1:p.Val198=
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