ENST00000461280.2:n.1544G>C
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ENST00000684241.1:n.3079G>C
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ENST00000262186.10:c.2246G>C
MANE Select
|
ENSP00000262186.5:p.Gly749Ala
|
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ENST00000330883.9:c.1226G>C
|
ENSP00000328531.4:p.Gly409Ala
|
|
ENST00000262186.9:c.2246G>C
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ENSP00000262186.5:p.Gly749Ala
|
|
ENST00000330883.8:c.1226G>C
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ENSP00000328531.4:p.Gly409Ala
|
|
ENST00000430723.4:c.1898G>C
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ENSP00000387657.4:p.Gly633Ala
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ENST00000461280.1:n.1533G>C
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ENST00000473610.5:n.1878G>C
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|
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ENST00000532957.5:n.2469G>C
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|
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NM_000238.3:c.2246G>C , LRG_288t1:c.2246G>C
|
NP_000229.1:p.Gly749Ala
|
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NM_001204798.1:c.1226G>C
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NP_001191727.1:p.Gly409Ala
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NM_172056.2:c.2246G>C , LRG_288t2:c.2246G>C
|
NP_742053.1:p.Gly749Ala
|
|
NM_172057.2:c.1226G>C , LRG_288t3:c.1226G>C
|
NP_742054.1:p.Gly409Ala
|
|
XM_011516185.1:c.1946G>C
|
XP_011514487.1:p.Gly649Ala
|
|
XM_011516186.1:c.2246G>C
|
XP_011514488.1:p.Gly749Ala
|
|
XM_011516185.2:c.1946G>C
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XP_011514487.1:p.Gly649Ala
|
|
XM_011516186.3:c.2246G>C
|
XP_011514488.1:p.Gly749Ala
|
|
XM_017012195.1:c.2096G>C
|
XP_016867684.1:p.Gly699Ala
|
|
XM_017012196.1:c.2069G>C
|
XP_016867685.1:p.Gly690Ala
|
|
NM_000238.4:c.2246G>C
MANE Select
|
NP_000229.1:p.Gly749Ala
|
|
NM_001204798.2:c.1226G>C
|
NP_001191727.1:p.Gly409Ala
|
|
NM_172057.3:c.1226G>C
|
NP_742054.1:p.Gly409Ala
|
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