ENST00000684241.1:n.3533G>A
|
|
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ENST00000262186.10:c.2700G>A
MANE Select
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ENSP00000262186.5:p.Glu900=
|
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ENST00000330883.9:c.1680G>A
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ENSP00000328531.4:p.Glu560=
|
|
ENST00000262186.9:c.2700G>A
|
ENSP00000262186.5:p.Glu900=
|
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ENST00000330883.8:c.1680G>A
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ENSP00000328531.4:p.Glu560=
|
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NM_000238.3:c.2700G>A , LRG_288t1:c.2700G>A
|
NP_000229.1:p.Glu900=
|
|
NM_172057.2:c.1680G>A , LRG_288t3:c.1680G>A
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NP_742054.1:p.Glu560=
|
|
XM_011516185.1:c.2400G>A
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XP_011514487.1:p.Glu800=
|
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XM_011516186.1:c.2693-180G>A
|
XP_011514488.1:n.2693-180G>A
|
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XM_011516185.2:c.2400G>A
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XP_011514487.1:p.Glu800=
|
|
XM_011516186.3:c.2693-180G>A
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XP_011514488.1:n.2693-180G>A
|
|
XM_017012195.1:c.2550G>A
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XP_016867684.1:p.Glu850=
|
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XM_017012196.1:c.2523G>A
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XP_016867685.1:p.Glu841=
|
|
NM_000238.4:c.2700G>A
MANE Select
|
NP_000229.1:p.Glu900=
|
|
NM_172057.3:c.1680G>A
|
NP_742054.1:p.Glu560=
|
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