ENST00000265631.10:c.1177G=
MANE Select
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ENSP00000265631.6:p.Gly393=
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ENST00000265631.9:c.1177G=
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ENSP00000265631.5:p.Gly393=
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|
ENST00000416240.6:c.1180G=
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ENSP00000400101.2:p.Gly394=
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ENST00000484495.5:n.330G=
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|
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ENST00000490072.5:n.244G=
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|
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ENST00000492869.1:n.298G=
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|
|
NM_001160210.1:c.1180G=
|
NP_001153682.1:p.Gly394=
|
|
NM_014251.2:c.1177G=
|
NP_055066.1:p.Gly393=
|
|
NR_027662.1:n.1252G=
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|
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XM_006715831.2:c.1210G=
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XP_006715894.1:p.Gly404=
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XM_011515727.1:c.1210G=
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XP_011514029.1:p.Gly404=
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|
XM_011515728.1:c.325G=
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XP_011514030.1:p.Gly109=
|
|
XM_006715831.4:c.1210G=
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XP_006715894.1:p.Gly404=
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|
XM_011515727.3:c.1210G=
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XP_011514029.1:p.Gly404=
|
|
XM_017011663.1:c.1168G=
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XP_016867152.1:p.Gly390=
|
|
XM_017011664.2:c.325G=
|
XP_016867153.1:p.Gly109=
|
|
XM_017011665.1:c.325G=
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XP_016867154.1:p.Gly109=
|
|
XR_001744525.2:n.1348G=
|
|
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XR_002956405.1:n.1981G=
|
|
|
NM_014251.3:c.1177G=
MANE Select
|
NP_055066.1:p.Gly393=
|
|
NR_027662.2:n.1203G=
|
|
|
NM_001160210.2:c.1180G=
|
NP_001153682.1:p.Gly394=
|
|