ENST00000684241.1:n.3465G>T
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|
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ENST00000262186.10:c.2632G>T
MANE Select
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ENSP00000262186.5:p.Glu878Ter
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ENST00000330883.9:c.1612G>T
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ENSP00000328531.4:p.Glu538Ter
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|
ENST00000262186.9:c.2632G>T
|
ENSP00000262186.5:p.Glu878Ter
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ENST00000330883.8:c.1612G>T
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ENSP00000328531.4:p.Glu538Ter
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NM_000238.3:c.2632G>T , LRG_288t1:c.2632G>T
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NP_000229.1:p.Glu878Ter
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NM_172057.2:c.1612G>T , LRG_288t3:c.1612G>T
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NP_742054.1:p.Glu538Ter
|
|
XM_011516185.1:c.2332G>T
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XP_011514487.1:p.Glu778Ter
|
|
XM_011516186.1:c.2632G>T
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XP_011514488.1:p.Glu878Ter
|
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XM_011516185.2:c.2332G>T
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XP_011514487.1:p.Glu778Ter
|
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XM_011516186.3:c.2632G>T
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XP_011514488.1:p.Glu878Ter
|
|
XM_017012195.1:c.2482G>T
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XP_016867684.1:p.Glu828Ter
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|
XM_017012196.1:c.2455G>T
|
XP_016867685.1:p.Glu819Ter
|
|
NM_000238.4:c.2632G>T
MANE Select
|
NP_000229.1:p.Glu878Ter
|
|
NM_172057.3:c.1612G>T
|
NP_742054.1:p.Glu538Ter
|
|