ENST00000311907.10:c.992C=
MANE Select
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ENSP00000308541.5:p.Ser331=
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ENST00000311907.9:c.992C=
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ENSP00000308541.5:p.Ser331=
|
|
ENST00000442468.1:c.962C=
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ENSP00000387413.1:p.Ser321=
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|
ENST00000530231.5:c.992C=
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ENSP00000433907.1:p.Ser331=
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|
NM_000506.3:c.992C=
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NP_000497.1:p.Ser331=
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|
NM_000506.4:c.992C= , LRG_551t1:c.992C=
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NP_000497.1:p.Ser331=
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|
NM_001311257.1:c.944C=
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NP_001298186.1:p.Ser315=
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XR_428840.2:n.1036C=
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|
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XR_428840.4:n.1027C=
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|
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NM_000506.5:c.992C=
MANE Select
|
NP_000497.1:p.Ser331=
|
|
NM_001311257.2:c.944C=
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NP_001298186.1:p.Ser315=
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|