|
ENST00000326735.13:c.3392C>G
MANE Select
|
ENSP00000327214.8:p.Ala1131Gly
|
|
|
ENST00000326735.12:c.3392C>G
|
ENSP00000327214.8:p.Ala1131Gly
|
|
|
ENST00000341676.9:c.3104-118C>G
|
ENSP00000341115.5:n.3104-118C>G
|
|
|
ENST00000452699.5:c.3377C>G
|
ENSP00000413307.1:p.Ala1126Gly
|
|
|
ENST00000466561.1:n.1438C>G
|
|
|
|
ENST00000502418.1:c.824-118C>G
|
ENSP00000423065.1:n.824-118C>G
|
|
|
NM_001141973.2:c.3377C>G
|
NP_001135445.1:p.Ala1126Gly
|
|
|
NM_001141974.2:c.3104-118C>G
|
NP_001135446.1:n.3104-118C>G
|
|
|
NM_022089.3:c.3392C>G
|
NP_071372.1:p.Ala1131Gly
|
|
|
XM_005245809.1:c.3236-118C>G
|
XP_005245866.1:n.3236-118C>G
|
|
|
XM_005245810.1:c.3233-118C>G
|
XP_005245867.1:n.3233-118C>G
|
|
|
XM_005245811.1:c.3221-118C>G
|
XP_005245868.1:n.3221-118C>G
|
|
|
XM_005245812.1:c.3209-118C>G
|
XP_005245869.1:n.3209-118C>G
|
|
|
XM_005245813.1:c.3176-118C>G
|
XP_005245870.1:n.3176-118C>G
|
|
|
XM_005245815.1:c.3119-118C>G
|
XP_005245872.1:n.3119-118C>G
|
|
|
XM_006710512.1:c.3218-118C>G
|
XP_006710575.1:n.3218-118C>G
|
|
|
XM_006710513.1:c.3194-118C>G
|
XP_006710576.1:n.3194-118C>G
|
|
|
XM_011541128.1:c.3221-118C>G
|
XP_011539430.1:n.3221-118C>G
|
|
|
XM_011541129.1:c.3029-118C>G
|
XP_011539431.1:n.3029-118C>G
|
|
|
XM_017000844.1:c.3377C>G
|
XP_016856333.1:p.Ala1126Gly
|
|
|
XM_017000845.1:c.3374C>G
|
XP_016856334.1:p.Ala1125Gly
|
|
|
XM_017000846.1:c.3350C>G
|
XP_016856335.1:p.Ala1117Gly
|
|
|
XM_017000847.1:c.3347C>G
|
XP_016856336.1:p.Ala1116Gly
|
|
|
XM_017000848.1:c.3275C>G
|
XP_016856337.1:p.Ala1092Gly
|
|
|
XM_017000849.1:c.3260C>G
|
XP_016856338.1:p.Ala1087Gly
|
|
|
XM_017000850.1:c.3185C>G
|
XP_016856339.1:p.Ala1062Gly
|
|
|
NM_022089.4:c.3392C>G
MANE Select
|
NP_071372.1:p.Ala1131Gly
|
|
|
NM_001141973.3:c.3377C>G
|
NP_001135445.1:p.Ala1126Gly
|
|
|
NM_001141974.3:c.3104-118C>G
|
NP_001135446.1:n.3104-118C>G
|
|
