ENST00000323929.8:c.441T>A
MANE Select
|
ENSP00000325863.4:p.Ala147=
|
|
ENST00000323929.7:c.441T>A
|
ENSP00000325863.3:p.Ala147=
|
|
ENST00000323977.7:c.441T>A
|
ENSP00000326094.3:p.Ala147=
|
|
ENST00000393241.8:c.441T>A
|
ENSP00000376933.4:p.Ala147=
|
|
ENST00000407439.7:c.450T>A
|
ENSP00000385614.3:p.Ala150=
|
|
ENST00000540013.5:c.441T>A
|
ENSP00000440986.1:p.Ala147=
|
|
ENST00000541157.5:n.517T>A
|
|
|
NM_005590.3:c.441T>A
|
NP_005581.2:p.Ala147=
|
|
NM_005591.3:c.441T>A , LRG_85t1:c.441T>A
|
NP_005582.1:p.Ala147=
|
|
XM_005274008.2:c.-28T>A
|
XP_005274065.1:n.-28T>A
|
|
XM_006718842.2:c.441T>A
|
XP_006718905.1:p.Ala147=
|
|
XM_011542837.1:c.441T>A
|
XP_011541139.1:p.Ala147=
|
|
XR_947828.1:n.737T>A
|
|
|
NM_001330347.1:c.441T>A
|
NP_001317276.1:p.Ala147=
|
|
XM_005274008.3:c.-28T>A
|
XP_005274065.1:n.-28T>A
|
|
XM_006718842.3:c.441T>A
|
XP_006718905.1:p.Ala147=
|
|
XM_011542837.2:c.441T>A
|
XP_011541139.1:p.Ala147=
|
|
XM_017017772.1:c.441T>A
|
XP_016873261.1:p.Ala147=
|
|
XR_947828.2:n.737T>A
|
|
|
NM_001330347.2:c.441T>A
|
NP_001317276.1:p.Ala147=
|
|
NM_005590.4:c.441T>A
|
NP_005581.2:p.Ala147=
|
|
NM_005591.4:c.441T>A
MANE Select
|
NP_005582.1:p.Ala147=
|
|