ENST00000684241.1:n.3910C>G
|
|
|
ENST00000262186.10:c.3077C>G
MANE Select
|
ENSP00000262186.5:p.Pro1026Arg
|
|
ENST00000330883.9:c.2057C>G
|
ENSP00000328531.4:p.Pro686Arg
|
|
ENST00000262186.9:c.3077C>G
|
ENSP00000262186.5:p.Pro1026Arg
|
|
ENST00000330883.8:c.2057C>G
|
ENSP00000328531.4:p.Pro686Arg
|
|
NM_000238.3:c.3077C>G , LRG_288t1:c.3077C>G
|
NP_000229.1:p.Pro1026Arg
|
|
NM_172057.2:c.2057C>G , LRG_288t3:c.2057C>G
|
NP_742054.1:p.Pro686Arg
|
|
XM_011516185.1:c.2777C>G
|
XP_011514487.1:p.Pro926Arg
|
|
XM_011516185.2:c.2777C>G
|
XP_011514487.1:p.Pro926Arg
|
|
XM_017012195.1:c.2927C>G
|
XP_016867684.1:p.Pro976Arg
|
|
XM_017012196.1:c.2900C>G
|
XP_016867685.1:p.Pro967Arg
|
|
NM_000238.4:c.3077C>G
MANE Select
|
NP_000229.1:p.Pro1026Arg
|
|
NM_172057.3:c.2057C>G
|
NP_742054.1:p.Pro686Arg
|
|