ENST00000684241.1:n.1390G>T
|
|
|
ENST00000262186.10:c.557G>T
MANE Select
|
ENSP00000262186.5:p.Gly186Val
|
|
ENST00000262186.9:c.557G>T
|
ENSP00000262186.5:p.Gly186Val
|
|
ENST00000430723.4:c.235-26G>T
|
ENSP00000387657.4:n.235-26G>T
|
|
ENST00000532957.5:n.780G>T
|
|
|
NM_000238.3:c.557G>T , LRG_288t1:c.557G>T
|
NP_000229.1:p.Gly186Val
|
|
NM_172056.2:c.557G>T , LRG_288t2:c.557G>T
|
NP_742053.1:p.Gly186Val
|
|
XM_011516185.1:c.257G>T
|
XP_011514487.1:p.Gly86Val
|
|
XM_011516186.1:c.557G>T
|
XP_011514488.1:p.Gly186Val
|
|
XM_011516185.2:c.257G>T
|
XP_011514487.1:p.Gly86Val
|
|
XM_011516186.3:c.557G>T
|
XP_011514488.1:p.Gly186Val
|
|
XM_017012195.1:c.407G>T
|
XP_016867684.1:p.Gly136Val
|
|
XM_017012196.1:c.380G>T
|
XP_016867685.1:p.Gly127Val
|
|
NM_000238.4:c.557G>T
MANE Select
|
NP_000229.1:p.Gly186Val
|
|