ENST00000684241.1:n.4273C>A
|
|
|
ENST00000262186.10:c.3440C>A
MANE Select
|
ENSP00000262186.5:p.Ser1147Tyr
|
|
ENST00000330883.9:c.2420C>A
|
ENSP00000328531.4:p.Ser807Tyr
|
|
ENST00000262186.9:c.3440C>A
|
ENSP00000262186.5:p.Ser1147Tyr
|
|
ENST00000330883.8:c.2420C>A
|
ENSP00000328531.4:p.Ser807Tyr
|
|
NM_000238.3:c.3440C>A , LRG_288t1:c.3440C>A
|
NP_000229.1:p.Ser1147Tyr
|
|
NM_172057.2:c.2420C>A , LRG_288t3:c.2420C>A
|
NP_742054.1:p.Ser807Tyr
|
|
XM_011516185.1:c.3140C>A
|
XP_011514487.1:p.Ser1047Tyr
|
|
XM_011516185.2:c.3140C>A
|
XP_011514487.1:p.Ser1047Tyr
|
|
XM_017012195.1:c.3290C>A
|
XP_016867684.1:p.Ser1097Tyr
|
|
XM_017012196.1:c.3263C>A
|
XP_016867685.1:p.Ser1088Tyr
|
|
NM_000238.4:c.3440C>A
MANE Select
|
NP_000229.1:p.Ser1147Tyr
|
|
NM_172057.3:c.2420C>A
|
NP_742054.1:p.Ser807Tyr
|
|