ENST00000265104.5:c.9740T>G
MANE Select
|
ENSP00000265104.4:p.Met3247Arg
|
|
ENST00000681290.1:c.9695T>G
|
ENSP00000505288.1:p.Met3232Arg
|
|
ENST00000265104.4:c.9740T>G
|
ENSP00000265104.4:p.Met3247Arg
|
|
ENST00000504001.3:n.452T>G
|
|
|
NM_001369.2:c.9740T>G
|
NP_001360.1:p.Met3247Arg
|
|
XM_005248262.2:c.9695T>G
|
XP_005248319.1:p.Met3232Arg
|
|
XM_005248262.3:c.9848T>G
|
XP_005248319.2:p.Met3283Arg
|
|
XM_017009177.1:c.9848T>G
|
XP_016864666.1:p.Met3283Arg
|
|
XM_017009178.1:c.8753T>G
|
XP_016864667.1:p.Met2918Arg
|
|
XM_017009179.2:c.8753T>G
|
XP_016864668.1:p.Met2918Arg
|
|
XM_017009180.1:c.9848T>G
|
XP_016864669.1:p.Met3283Arg
|
|
XM_017009181.1:c.9848T>G
|
XP_016864670.1:p.Met3283Arg
|
|
XM_017009182.1:c.9848T>G
|
XP_016864671.1:p.Met3283Arg
|
|
XM_017009185.1:c.4937T>G
|
XP_016864674.1:p.Met1646Arg
|
|
XM_017009186.1:c.4490T>G
|
XP_016864675.1:p.Met1497Arg
|
|
XM_017009188.1:c.3827T>G
|
XP_016864677.1:p.Met1276Arg
|
|
XM_024454388.1:c.8753T>G
|
XP_024310156.1:p.Met2918Arg
|
|
XM_024454389.1:c.8342T>G
|
XP_024310157.1:p.Met2781Arg
|
|
NM_001369.3:c.9740T>G
MANE Select
|
NP_001360.1:p.Met3247Arg
|
|