ENST00000684241.1:n.1757G=
|
|
|
ENST00000262186.10:c.924G=
MANE Select
|
ENSP00000262186.5:p.Met308=
|
|
ENST00000262186.9:c.924G=
|
ENSP00000262186.5:p.Met308=
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|
ENST00000430723.4:c.576G=
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ENSP00000387657.4:p.Met192=
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|
ENST00000532957.5:n.1147G=
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|
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NM_000238.3:c.924G= , LRG_288t1:c.924G=
|
NP_000229.1:p.Met308=
|
|
NM_172056.2:c.924G= , LRG_288t2:c.924G=
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NP_742053.1:p.Met308=
|
|
XM_011516185.1:c.624G=
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XP_011514487.1:p.Met208=
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|
XM_011516186.1:c.924G=
|
XP_011514488.1:p.Met308=
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|
XM_011516185.2:c.624G=
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XP_011514487.1:p.Met208=
|
|
XM_011516186.3:c.924G=
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XP_011514488.1:p.Met308=
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|
XM_017012195.1:c.774G=
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XP_016867684.1:p.Met258=
|
|
XM_017012196.1:c.747G=
|
XP_016867685.1:p.Met249=
|
|
NM_000238.4:c.924G=
MANE Select
|
NP_000229.1:p.Met308=
|
|