ENST00000432791.7:c.2899C>A
MANE Select
|
ENSP00000387393.3:p.Pro967Thr
|
|
ENST00000572904.6:c.2899C>A
|
ENSP00000461484.1:p.Pro967Thr
|
|
ENST00000574590.6:c.2896C>A
|
ENSP00000461812.2:p.Pro966Thr
|
|
ENST00000575318.6:c.2707C>A
|
ENSP00000461299.1:p.Pro903Thr
|
|
ENST00000638275.1:c.2707C>A
|
ENSP00000492576.1:p.Pro903Thr
|
|
ENST00000638291.1:n.727C>A
|
|
|
ENST00000638551.1:n.847C>A
|
|
|
ENST00000639467.1:c.556C>A
|
ENSP00000492741.1:p.Pro186Thr
|
|
ENST00000639805.1:n.316C>A
|
|
|
ENST00000648792.1:c.2838-71C>A
|
ENSP00000497628.1:n.2838-71C>A
|
|
ENST00000262419.10:c.2899C>A
|
ENSP00000262419.6:p.Pro967Thr
|
|
ENST00000432791.5:c.2896C>A
|
ENSP00000387393.2:p.Pro966Thr
|
|
ENST00000572218.5:n.7116C>A
|
|
|
ENST00000572904.5:c.2899C>A
|
ENSP00000461484.1:p.Pro967Thr
|
|
ENST00000573682.1:n.285C>A
|
|
|
ENST00000574590.5:c.2899C>A
|
ENSP00000461812.1:p.Pro967Thr
|
|
ENST00000574963.1:n.329C>A
|
|
|
ENST00000575318.5:c.2707C>A
|
ENSP00000461299.1:p.Pro903Thr
|
|
ENST00000576870.5:n.871C>A
|
|
|
NM_001193465.1:c.2896C>A
|
NP_001180394.1:p.Pro966Thr
|
|
NM_001193466.1:c.2899C>A
|
NP_001180395.1:p.Pro967Thr
|
|
NM_015443.3:c.2899C>A
|
NP_056258.1:p.Pro967Thr
|
|
XM_006721823.1:c.2899C>A
|
XP_006721886.1:p.Pro967Thr
|
|
XM_006721824.2:c.2899C>A
|
XP_006721887.1:p.Pro967Thr
|
|
XM_011524628.1:c.2896C>A
|
XP_011522930.1:p.Pro966Thr
|
|
XM_011524629.1:c.2797C>A
|
XP_011522931.1:p.Pro933Thr
|
|
XM_011524630.1:c.2710C>A
|
XP_011522932.1:p.Pro904Thr
|
|
XM_011524631.1:c.2707C>A
|
XP_011522933.1:p.Pro903Thr
|
|
XM_011524632.1:c.1669C>A
|
XP_011522934.1:p.Pro557Thr
|
|
XM_006721823.2:c.2899C>A
|
XP_006721886.1:p.Pro967Thr
|
|
XM_006721824.4:c.2899C>A
|
XP_006721887.1:p.Pro967Thr
|
|
XM_011524628.3:c.2896C>A
|
XP_011522930.1:p.Pro966Thr
|
|
XM_011524629.3:c.2797C>A
|
XP_011522931.1:p.Pro933Thr
|
|
XM_011524630.3:c.2710C>A
|
XP_011522932.1:p.Pro904Thr
|
|
XM_011524631.3:c.2707C>A
|
XP_011522933.1:p.Pro903Thr
|
|
XM_011524632.3:c.1669C>A
|
XP_011522934.1:p.Pro557Thr
|
|
XM_017024488.2:c.2707C>A
|
XP_016879977.1:p.Pro903Thr
|
|
NM_001193466.2:c.2899C>A
|
NP_001180395.1:p.Pro967Thr
|
|
NM_015443.4:c.2899C>A
MANE Select
|
NP_056258.1:p.Pro967Thr
|
|
NM_001193465.2:c.2896C>A
|
NP_001180394.1:p.Pro966Thr
|
|
NM_001379198.1:c.2899C>A
|
NP_001366127.1:p.Pro967Thr
|
|