ENST00000311907.10:c.926G>T
MANE Select
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ENSP00000308541.5:p.Arg309Met
|
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ENST00000311907.9:c.926G>T
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ENSP00000308541.5:p.Arg309Met
|
|
ENST00000442468.1:c.896G>T
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ENSP00000387413.1:p.Arg299Met
|
|
ENST00000530231.5:c.926G>T
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ENSP00000433907.1:p.Arg309Met
|
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NM_000506.3:c.926G>T
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NP_000497.1:p.Arg309Met
|
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NM_000506.4:c.926G>T , LRG_551t1:c.926G>T
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NP_000497.1:p.Arg309Met
|
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NM_001311257.1:c.878G>T
|
NP_001298186.1:p.Arg293Met
|
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XR_428840.2:n.970G>T
|
|
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XR_428840.4:n.961G>T
|
|
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NM_000506.5:c.926G>T
MANE Select
|
NP_000497.1:p.Arg309Met
|
|
NM_001311257.2:c.878G>T
|
NP_001298186.1:p.Arg293Met
|
|