ENST00000684241.1:n.1647T>G
|
|
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ENST00000262186.10:c.814T>G
MANE Select
|
ENSP00000262186.5:p.Ser272Ala
|
|
ENST00000262186.9:c.814T>G
|
ENSP00000262186.5:p.Ser272Ala
|
|
ENST00000430723.4:c.466T>G
|
ENSP00000387657.4:p.Ser156Ala
|
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ENST00000532957.5:n.1037T>G
|
|
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NM_000238.3:c.814T>G , LRG_288t1:c.814T>G
|
NP_000229.1:p.Ser272Ala
|
|
NM_172056.2:c.814T>G , LRG_288t2:c.814T>G
|
NP_742053.1:p.Ser272Ala
|
|
XM_011516185.1:c.514T>G
|
XP_011514487.1:p.Ser172Ala
|
|
XM_011516186.1:c.814T>G
|
XP_011514488.1:p.Ser272Ala
|
|
XM_011516185.2:c.514T>G
|
XP_011514487.1:p.Ser172Ala
|
|
XM_011516186.3:c.814T>G
|
XP_011514488.1:p.Ser272Ala
|
|
XM_017012195.1:c.664T>G
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XP_016867684.1:p.Ser222Ala
|
|
XM_017012196.1:c.637T>G
|
XP_016867685.1:p.Ser213Ala
|
|
NM_000238.4:c.814T>G
MANE Select
|
NP_000229.1:p.Ser272Ala
|
|