ENST00000311907.10:c.562C>T
MANE Select
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ENSP00000308541.5:p.Gln188Ter
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ENST00000311907.9:c.562C>T
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ENSP00000308541.5:p.Gln188Ter
|
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ENST00000442468.1:c.532C>T
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ENSP00000387413.1:p.Gln178Ter
|
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ENST00000490274.1:n.342C>T
|
|
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ENST00000530231.5:c.562C>T
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ENSP00000433907.1:p.Gln188Ter
|
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NM_000506.3:c.562C>T
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NP_000497.1:p.Gln188Ter
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NM_000506.4:c.562C>T , LRG_551t1:c.562C>T
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NP_000497.1:p.Gln188Ter
|
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NM_001311257.1:c.514C>T
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NP_001298186.1:p.Gln172Ter
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XR_428840.2:n.606C>T
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|
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XR_428840.4:n.597C>T
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|
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NM_000506.5:c.562C>T
MANE Select
|
NP_000497.1:p.Gln188Ter
|
|
NM_001311257.2:c.514C>T
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NP_001298186.1:p.Gln172Ter
|
|