ENST00000684241.1:n.3564G>T
|
|
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ENST00000262186.10:c.2731G>T
MANE Select
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ENSP00000262186.5:p.Gly911Cys
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|
ENST00000330883.9:c.1711G>T
|
ENSP00000328531.4:p.Gly571Cys
|
|
ENST00000262186.9:c.2731G>T
|
ENSP00000262186.5:p.Gly911Cys
|
|
ENST00000330883.8:c.1711G>T
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ENSP00000328531.4:p.Gly571Cys
|
|
NM_000238.3:c.2731G>T , LRG_288t1:c.2731G>T
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NP_000229.1:p.Gly911Cys
|
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NM_172057.2:c.1711G>T , LRG_288t3:c.1711G>T
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NP_742054.1:p.Gly571Cys
|
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XM_011516185.1:c.2431G>T
|
XP_011514487.1:p.Gly811Cys
|
|
XM_011516186.1:c.2693-149G>T
|
XP_011514488.1:n.2693-149G>T
|
|
XM_011516185.2:c.2431G>T
|
XP_011514487.1:p.Gly811Cys
|
|
XM_011516186.3:c.2693-149G>T
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XP_011514488.1:n.2693-149G>T
|
|
XM_017012195.1:c.2581G>T
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XP_016867684.1:p.Gly861Cys
|
|
XM_017012196.1:c.2554G>T
|
XP_016867685.1:p.Gly852Cys
|
|
NM_000238.4:c.2731G>T
MANE Select
|
NP_000229.1:p.Gly911Cys
|
|
NM_172057.3:c.1711G>T
|
NP_742054.1:p.Gly571Cys
|
|