ENST00000650516.2:c.676G>T
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ENSP00000498052.2:p.Gly226Cys
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ENST00000343257.7:c.676G>T
MANE Select
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ENSP00000339867.2:p.Gly226Cys
|
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ENST00000432192.6:c.444G>T
|
|
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ENST00000455478.6:c.130G>T
|
ENSP00000400027.2:p.Gly44Cys
|
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ENST00000650516.1:c.676G>T
|
ENSP00000498052.1:p.Gly226Cys
|
|
ENST00000343257.6:c.676G>T
|
ENSP00000339867.2:p.Gly226Cys
|
|
ENST00000432192.5:c.134G>T
|
|
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ENST00000455478.5:c.134G>T
|
|
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ENST00000495612.1:n.134G>T
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|
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NM_000083.2:c.676G>T
|
NP_000074.2:p.Gly226Cys
|
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NR_046453.1:n.763G>T
|
|
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XM_011515781.1:c.676G>T
|
XP_011514083.1:p.Gly226Cys
|
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XM_017011739.1:c.383G>T
|
XP_016867228.1:p.Trp128Leu
|
|
XM_017011740.1:c.383G>T
|
XP_016867229.1:p.Trp128Leu
|
|
NM_000083.3:c.676G>T
MANE Select
|
NP_000074.3:p.Gly226Cys
|
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NR_046453.2:n.778G>T
|
|
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