ENST00000684241.1:n.4169C>A
|
|
|
ENST00000262186.10:c.3336C>A
MANE Select
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ENSP00000262186.5:p.Ser1112=
|
|
ENST00000330883.9:c.2316C>A
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ENSP00000328531.4:p.Ser772=
|
|
ENST00000262186.9:c.3336C>A
|
ENSP00000262186.5:p.Ser1112=
|
|
ENST00000330883.8:c.2316C>A
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ENSP00000328531.4:p.Ser772=
|
|
NM_000238.3:c.3336C>A , LRG_288t1:c.3336C>A
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NP_000229.1:p.Ser1112=
|
|
NM_172057.2:c.2316C>A , LRG_288t3:c.2316C>A
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NP_742054.1:p.Ser772=
|
|
XM_011516185.1:c.3036C>A
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XP_011514487.1:p.Ser1012=
|
|
XM_011516185.2:c.3036C>A
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XP_011514487.1:p.Ser1012=
|
|
XM_017012195.1:c.3186C>A
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XP_016867684.1:p.Ser1062=
|
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XM_017012196.1:c.3159C>A
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XP_016867685.1:p.Ser1053=
|
|
NM_000238.4:c.3336C>A
MANE Select
|
NP_000229.1:p.Ser1112=
|
|
NM_172057.3:c.2316C>A
|
NP_742054.1:p.Ser772=
|
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