ENST00000684241.1:n.1945C>A
|
|
|
ENST00000262186.10:c.1112C>A
MANE Select
|
ENSP00000262186.5:p.Thr371Asn
|
|
ENST00000262186.9:c.1112C>A
|
ENSP00000262186.5:p.Thr371Asn
|
|
ENST00000430723.4:c.764C>A
|
ENSP00000387657.4:p.Thr255Asn
|
|
ENST00000532957.5:n.1335C>A
|
|
|
NM_000238.3:c.1112C>A , LRG_288t1:c.1112C>A
|
NP_000229.1:p.Thr371Asn
|
|
NM_172056.2:c.1112C>A , LRG_288t2:c.1112C>A
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NP_742053.1:p.Thr371Asn
|
|
XM_011516185.1:c.812C>A
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XP_011514487.1:p.Thr271Asn
|
|
XM_011516186.1:c.1112C>A
|
XP_011514488.1:p.Thr371Asn
|
|
XM_011516185.2:c.812C>A
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XP_011514487.1:p.Thr271Asn
|
|
XM_011516186.3:c.1112C>A
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XP_011514488.1:p.Thr371Asn
|
|
XM_017012195.1:c.962C>A
|
XP_016867684.1:p.Thr321Asn
|
|
XM_017012196.1:c.935C>A
|
XP_016867685.1:p.Thr312Asn
|
|
NM_000238.4:c.1112C>A
MANE Select
|
NP_000229.1:p.Thr371Asn
|
|