ENST00000311907.10:c.638G>C
MANE Select
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ENSP00000308541.5:p.Cys213Ser
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|
ENST00000311907.9:c.638G>C
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ENSP00000308541.5:p.Cys213Ser
|
|
ENST00000442468.1:c.608G>C
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ENSP00000387413.1:p.Cys203Ser
|
|
ENST00000490274.1:n.418G>C
|
|
|
ENST00000530231.5:c.638G>C
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ENSP00000433907.1:p.Cys213Ser
|
|
NM_000506.3:c.638G>C
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NP_000497.1:p.Cys213Ser
|
|
NM_000506.4:c.638G>C , LRG_551t1:c.638G>C
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NP_000497.1:p.Cys213Ser
|
|
NM_001311257.1:c.590G>C
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NP_001298186.1:p.Cys197Ser
|
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XR_428840.2:n.682G>C
|
|
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XR_428840.4:n.673G>C
|
|
|
NM_000506.5:c.638G>C
MANE Select
|
NP_000497.1:p.Cys213Ser
|
|
NM_001311257.2:c.590G>C
|
NP_001298186.1:p.Cys197Ser
|
|