ENST00000432791.7:c.3298C>T
MANE Select
|
ENSP00000387393.3:p.Gln1100Ter
|
|
ENST00000572904.6:c.3298C>T
|
ENSP00000461484.1:p.Gln1100Ter
|
|
ENST00000574590.6:c.3295C>T
|
ENSP00000461812.2:p.Gln1099Ter
|
|
ENST00000575318.6:c.3106C>T
|
ENSP00000461299.1:p.Gln1036Ter
|
|
ENST00000638275.1:c.3106C>T
|
ENSP00000492576.1:p.Gln1036Ter
|
|
ENST00000648792.1:c.3166C>T
|
ENSP00000497628.1:p.Gln1056Ter
|
|
ENST00000262419.10:c.3298C>T
|
ENSP00000262419.6:p.Gln1100Ter
|
|
ENST00000432791.5:c.3295C>T
|
ENSP00000387393.2:p.Gln1099Ter
|
|
ENST00000572218.5:n.7515C>T
|
|
|
ENST00000572904.5:c.3298C>T
|
ENSP00000461484.1:p.Gln1100Ter
|
|
ENST00000574590.5:c.3298C>T
|
ENSP00000461812.1:p.Gln1100Ter
|
|
ENST00000574963.1:n.1071C>T
|
|
|
ENST00000575318.5:c.3106C>T
|
ENSP00000461299.1:p.Gln1036Ter
|
|
ENST00000576870.5:n.1270C>T
|
|
|
NM_001193465.1:c.3295C>T
|
NP_001180394.1:p.Gln1099Ter
|
|
NM_001193466.1:c.3298C>T
|
NP_001180395.1:p.Gln1100Ter
|
|
NM_015443.3:c.3298C>T
|
NP_056258.1:p.Gln1100Ter
|
|
XM_006721823.1:c.3298C>T
|
XP_006721886.1:p.Gln1100Ter
|
|
XM_006721824.2:c.3298C>T
|
XP_006721887.1:p.Gln1100Ter
|
|
XM_011524628.1:c.3295C>T
|
XP_011522930.1:p.Gln1099Ter
|
|
XM_011524629.1:c.3196C>T
|
XP_011522931.1:p.Gln1066Ter
|
|
XM_011524630.1:c.3109C>T
|
XP_011522932.1:p.Gln1037Ter
|
|
XM_011524631.1:c.3106C>T
|
XP_011522933.1:p.Gln1036Ter
|
|
XM_011524632.1:c.2068C>T
|
XP_011522934.1:p.Gln690Ter
|
|
XM_006721823.2:c.3298C>T
|
XP_006721886.1:p.Gln1100Ter
|
|
XM_006721824.4:c.3298C>T
|
XP_006721887.1:p.Gln1100Ter
|
|
XM_011524628.3:c.3295C>T
|
XP_011522930.1:p.Gln1099Ter
|
|
XM_011524629.3:c.3196C>T
|
XP_011522931.1:p.Gln1066Ter
|
|
XM_011524630.3:c.3109C>T
|
XP_011522932.1:p.Gln1037Ter
|
|
XM_011524631.3:c.3106C>T
|
XP_011522933.1:p.Gln1036Ter
|
|
XM_011524632.3:c.2068C>T
|
XP_011522934.1:p.Gln690Ter
|
|
XM_017024488.2:c.3106C>T
|
XP_016879977.1:p.Gln1036Ter
|
|
NM_001193466.2:c.3298C>T
|
NP_001180395.1:p.Gln1100Ter
|
|
NM_015443.4:c.3298C>T
MANE Select
|
NP_056258.1:p.Gln1100Ter
|
|
NM_001193465.2:c.3295C>T
|
NP_001180394.1:p.Gln1099Ter
|
|
NM_001379198.1:c.3298C>T
|
NP_001366127.1:p.Gln1100Ter
|
|