|
ENST00000235521.5:c.4G>T
(WARS2)
MANE Select
|
ENSP00000235521.4:p.Ala2Ser
|
|
|
ENST00000235521.4:c.4G>T
(WARS2)
|
ENSP00000235521.4:p.Ala2Ser
|
|
|
ENST00000369426.9:c.4G>T
(WARS2)
|
ENSP00000358434.5:p.Ala2Ser
|
|
|
ENST00000495746.5:n.14G>T
(WARS2)
|
|
|
|
NM_015836.3:c.4G>T
(WARS2)
|
NP_056651.1:p.Ala2Ser
|
|
|
NM_201263.2:c.4G>T
(WARS2)
|
NP_957715.1:p.Ala2Ser
|
|
|
NR_125974.1:n.246C>A
(WARS2-AS1)
|
|
|
|
NR_125975.1:n.246C>A
(WARS2-AS1)
|
|
|
|
NR_125976.1:n.246C>A
(WARS2-AS1)
|
|
|
|
NR_125977.1:n.246C>A
(WARS2-AS1)
|
|
|
|
XM_006710283.1:c.-566G>T
(WARS2)
|
XP_006710346.1:n.-566G>T
|
|
|
XM_011540493.1:c.-438G>T
(WARS2)
|
XP_011538795.1:n.-438G>T
|
|
|
XM_011540494.1:c.-151G>T
(WARS2)
|
XP_011538796.1:n.-151G>T
|
|
|
XM_011540495.1:c.4G>T
(WARS2)
|
XP_011538797.1:p.Ala2Ser
|
|
|
XM_011540494.2:c.-151G>T
(WARS2)
|
XP_011538796.1:n.-151G>T
|
|
|
XM_011540495.2:c.4G>T
(WARS2)
|
XP_011538797.1:p.Ala2Ser
|
|
|
XM_017000038.1:c.4G>T
(WARS2)
|
XP_016855527.1:p.Ala2Ser
|
|
|
XM_017000039.1:c.-342G>T
(WARS2)
|
XP_016855528.1:n.-342G>T
|
|
|
XM_017000040.1:c.4G>T
(WARS2)
|
XP_016855529.1:p.Ala2Ser
|
|
|
XM_017000041.2:c.-566G>T
(WARS2)
|
XP_016855530.1:n.-566G>T
|
|
|
XM_017000042.1:c.4G>T
(WARS2)
|
XP_016855531.1:p.Ala2Ser
|
|
|
XM_024449826.1:c.-438G>T
(WARS2)
|
XP_024305594.1:n.-438G>T
|
|
|
XM_024449860.1:c.-566G>T
(WARS2)
|
XP_024305628.1:n.-566G>T
|
|
|
XM_024449871.1:c.-470G>T
(WARS2)
|
XP_024305639.1:n.-470G>T
|
|
|
NM_001378226.1:c.-151G>T
(WARS2)
|
NP_001365155.1:n.-151G>T
|
|
|
NM_001378227.1:c.-342G>T
(WARS2)
|
NP_001365156.1:n.-342G>T
|
|
|
NM_001378228.1:c.4G>T
(WARS2)
|
NP_001365157.1:p.Ala2Ser
|
|
|
NM_001378229.1:c.4G>T
(WARS2)
|
NP_001365158.1:p.Ala2Ser
|
|
|
NM_001378230.1:c.-470G>T
(WARS2)
|
NP_001365159.1:n.-470G>T
|
|
|
NM_001378231.1:c.4G>T
(WARS2)
|
NP_001365160.1:p.Ala2Ser
|
|
|
NM_015836.4:c.4G>T
(WARS2)
MANE Select
|
NP_056651.1:p.Ala2Ser
|
|
