ENST00000399503.4:c.754_757delinsTCTC
MANE Select
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ENSP00000382423.3:p.Ser252=
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ENST00000399503.3:c.754_757delinsTCTC
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ENSP00000382423.3:p.Ser252=
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|
NM_005921.1:c.754_757delinsTCTC
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NP_005912.1:p.Ser252=
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|
XM_005248519.3:c.376_379delinsTCTC
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XP_005248576.2:p.Ser126=
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XM_011543406.1:c.499_502delinsTCTC
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XP_011541708.1:p.Ser167=
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|
XM_011543407.1:c.754_757delinsTCTC
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XP_011541709.1:p.Ser252=
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|
XM_011543408.1:c.754_757delinsTCTC
|
XP_011541710.1:p.Ser252=
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XM_017009484.1:c.343_346delinsTCTC
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XP_016864973.1:p.Ser115=
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XM_017009485.1:c.265_268delinsTCTC
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XP_016864974.1:p.Ser89=
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|
XR_001742068.2:n.785_788delinsTCTC
|
|
|
NM_005921.2:c.754_757delinsTCTC
MANE Select
|
NP_005912.1:p.Ser252=
|
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