ENST00000326735.13:c.2560A>G
MANE Select
|
ENSP00000327214.8:p.Met854Val
|
|
ENST00000326735.12:c.2560A>G
|
ENSP00000327214.8:p.Met854Val
|
|
ENST00000341676.9:c.2428A>G
|
ENSP00000341115.5:p.Met810Val
|
|
ENST00000452699.5:c.2545A>G
|
ENSP00000413307.1:p.Met849Val
|
|
ENST00000466561.1:n.434A>G
|
|
|
ENST00000502418.1:c.148A>G
|
ENSP00000423065.1:p.Met50Val
|
|
NM_001141973.2:c.2545A>G
|
NP_001135445.1:p.Met849Val
|
|
NM_001141974.2:c.2428A>G
|
NP_001135446.1:p.Met810Val
|
|
NM_022089.3:c.2560A>G
|
NP_071372.1:p.Met854Val
|
|
XM_005245809.1:c.2560A>G
|
XP_005245866.1:p.Met854Val
|
|
XM_005245810.1:c.2557A>G
|
XP_005245867.1:p.Met853Val
|
|
XM_005245811.1:c.2545A>G
|
XP_005245868.1:p.Met849Val
|
|
XM_005245812.1:c.2533A>G
|
XP_005245869.1:p.Met845Val
|
|
XM_005245813.1:c.2500A>G
|
XP_005245870.1:p.Met834Val
|
|
XM_005245815.1:c.2443A>G
|
XP_005245872.1:p.Met815Val
|
|
XM_006710512.1:c.2542A>G
|
XP_006710575.1:p.Met848Val
|
|
XM_006710513.1:c.2518A>G
|
XP_006710576.1:p.Met840Val
|
|
XM_011541128.1:c.2545A>G
|
XP_011539430.1:p.Met849Val
|
|
XM_011541129.1:c.2353A>G
|
XP_011539431.1:p.Met785Val
|
|
XM_017000844.1:c.2545A>G
|
XP_016856333.1:p.Met849Val
|
|
XM_017000845.1:c.2542A>G
|
XP_016856334.1:p.Met848Val
|
|
XM_017000846.1:c.2518A>G
|
XP_016856335.1:p.Met840Val
|
|
XM_017000847.1:c.2515A>G
|
XP_016856336.1:p.Met839Val
|
|
XM_017000848.1:c.2443A>G
|
XP_016856337.1:p.Met815Val
|
|
XM_017000849.1:c.2428A>G
|
XP_016856338.1:p.Met810Val
|
|
XM_017000850.1:c.2353A>G
|
XP_016856339.1:p.Met785Val
|
|
NM_022089.4:c.2560A>G
MANE Select
|
NP_071372.1:p.Met854Val
|
|
NM_001141973.3:c.2545A>G
|
NP_001135445.1:p.Met849Val
|
|
NM_001141974.3:c.2428A>G
|
NP_001135446.1:p.Met810Val
|
|