ENST00000461280.2:n.655G>C
|
|
|
ENST00000684116.1:n.250G>C
|
|
|
ENST00000684241.1:n.2190G>C
|
|
|
ENST00000262186.10:c.1357G>C
MANE Select
|
ENSP00000262186.5:p.Ala453Pro
|
|
ENST00000330883.9:c.337G>C
|
ENSP00000328531.4:p.Ala113Pro
|
|
ENST00000262186.9:c.1357G>C
|
ENSP00000262186.5:p.Ala453Pro
|
|
ENST00000330883.8:c.337G>C
|
ENSP00000328531.4:p.Ala113Pro
|
|
ENST00000430723.4:c.1009G>C
|
ENSP00000387657.4:p.Ala337Pro
|
|
ENST00000461280.1:n.644G>C
|
|
|
ENST00000473610.5:n.662G>C
|
|
|
ENST00000532957.5:n.1580G>C
|
|
|
NM_000238.3:c.1357G>C , LRG_288t1:c.1357G>C
|
NP_000229.1:p.Ala453Pro
|
|
NM_001204798.1:c.337G>C
|
NP_001191727.1:p.Ala113Pro
|
|
NM_172056.2:c.1357G>C , LRG_288t2:c.1357G>C
|
NP_742053.1:p.Ala453Pro
|
|
NM_172057.2:c.337G>C , LRG_288t3:c.337G>C
|
NP_742054.1:p.Ala113Pro
|
|
XM_011516185.1:c.1057G>C
|
XP_011514487.1:p.Ala353Pro
|
|
XM_011516186.1:c.1357G>C
|
XP_011514488.1:p.Ala453Pro
|
|
XM_011516185.2:c.1057G>C
|
XP_011514487.1:p.Ala353Pro
|
|
XM_011516186.3:c.1357G>C
|
XP_011514488.1:p.Ala453Pro
|
|
XM_017012195.1:c.1207G>C
|
XP_016867684.1:p.Ala403Pro
|
|
XM_017012196.1:c.1180G>C
|
XP_016867685.1:p.Ala394Pro
|
|
NM_000238.4:c.1357G>C
MANE Select
|
NP_000229.1:p.Ala453Pro
|
|
NM_001204798.2:c.337G>C
|
NP_001191727.1:p.Ala113Pro
|
|
NM_172057.3:c.337G>C
|
NP_742054.1:p.Ala113Pro
|
|