|
ENST00000474905.6:c.832T>G
MANE Select
|
ENSP00000417314.1:p.Phe278Val
|
|
|
ENST00000393213.7:c.832T>G
|
ENSP00000376907.3:p.Phe278Val
|
|
|
ENST00000431780.6:c.832T>G
|
ENSP00000393045.2:p.Phe278Val
|
|
|
ENST00000461828.5:c.832T>G
|
ENSP00000418183.1:p.Phe278Val
|
|
|
ENST00000466363.6:c.832T>G
|
ENSP00000419025.2:p.Phe278Val
|
|
|
ENST00000474905.5:c.832T>G
|
ENSP00000417314.1:p.Phe278Val
|
|
|
ENST00000479492.1:c.63T>G
|
|
|
|
ENST00000485477.5:c.832T>G
|
ENSP00000420237.1:p.Phe278Val
|
|
|
ENST00000495736.1:n.1054T>G
|
|
|
|
NM_001127441.1:c.832T>G
|
NP_001120913.1:p.Phe278Val
|
|
|
NM_001127442.1:c.832T>G
|
NP_001120914.1:p.Phe278Val
|
|
|
NM_080385.4:c.832T>G
|
NP_525124.3:p.Phe278Val
|
|
|
XM_005250710.1:c.832T>G
|
XP_005250767.1:p.Phe278Val
|
|
|
XM_005250711.1:c.832T>G
|
XP_005250768.1:p.Phe278Val
|
|
|
XM_005250712.1:c.832T>G
|
XP_005250769.1:p.Phe278Val
|
|
|
XM_011516698.1:c.832T>G
|
XP_011515000.1:p.Phe278Val
|
|
|
XM_011516699.1:c.832T>G
|
XP_011515001.1:p.Phe278Val
|
|
|
XM_011516700.1:c.832T>G
|
XP_011515002.1:p.Phe278Val
|
|
|
XM_011516701.1:c.832T>G
|
XP_011515003.1:p.Phe278Val
|
|
|
XM_011516702.1:c.832T>G
|
XP_011515004.1:p.Phe278Val
|
|
|
XM_011516703.1:c.832T>G
|
XP_011515005.1:p.Phe278Val
|
|
|
XM_011516704.1:c.832T>G
|
XP_011515006.1:p.Phe278Val
|
|
|
XM_011516705.1:c.832T>G
|
XP_011515007.1:p.Phe278Val
|
|
|
XR_927548.1:n.2031T>G
|
|
|
|
XR_927549.1:n.2031T>G
|
|
|
|
XR_927550.1:n.2031T>G
|
|
|
|
XR_927551.1:n.2031T>G
|
|
|
|
NM_001318223.1:c.832T>G
|
NP_001305152.1:p.Phe278Val
|
|
|
XM_024446999.1:c.832T>G
|
XP_024302767.1:p.Phe278Val
|
|
|
XM_024447000.1:c.832T>G
|
XP_024302768.1:p.Phe278Val
|
|
|
XM_024447001.1:c.832T>G
|
XP_024302769.1:p.Phe278Val
|
|
|
NM_001127441.2:c.832T>G
|
NP_001120913.1:p.Phe278Val
|
|
|
NM_001127442.2:c.832T>G
|
NP_001120914.1:p.Phe278Val
|
|
|
NM_001318223.2:c.832T>G
|
NP_001305152.1:p.Phe278Val
|
|
|
NM_080385.5:c.832T>G
MANE Select
|
NP_525124.3:p.Phe278Val
|
|
