ENST00000636937.2:c.3493G>T
|
ENSP00000516154.1:p.Ala1165Ser
|
|
ENST00000268124.11:c.3493G>T
MANE Select
|
ENSP00000268124.5:p.Ala1165Ser
|
|
ENST00000530292.3:c.3193G>T
|
ENSP00000432885.2:n.3193G>T
|
|
ENST00000635986.2:c.*563G>T
|
ENSP00000490653.2:n.*563G>T
|
|
ENST00000636774.1:c.*2097G>T
|
ENSP00000489799.1:n.*2097G>T
|
|
ENST00000637042.1:n.72-55G>T
|
|
|
ENST00000637238.1:c.2401G>T
|
ENSP00000490756.1:n.2401G>T
|
|
ENST00000637264.1:c.2555-50G>T
|
|
|
ENST00000666746.1:c.3070G>T
|
|
|
ENST00000672071.1:n.4695G>T
|
|
|
ENST00000672695.1:n.1272G>T
|
|
|
ENST00000672923.2:n.3493G>T
|
|
|
ENST00000268124.9:c.3493G>T
|
ENSP00000268124.5:p.Ala1165Ser
|
|
ENST00000442287.6:c.3493G>T
|
ENSP00000399851.2:p.Ala1165Ser
|
|
ENST00000526671.1:n.303G>T
|
|
|
ENST00000530292.2:c.676G>T
|
ENSP00000432885.1:n.676G>T
|
|
ENST00000631044.2:c.*2917G>T
|
ENSP00000486730.1:n.*2917G>T
|
|
NM_001126131.1:c.3493G>T
|
NP_001119603.1:p.Ala1165Ser
|
|
NM_002693.2:c.3493G>T
|
NP_002684.1:p.Ala1165Ser
|
|
NM_001126131.2:c.3493G>T
|
NP_001119603.1:p.Ala1165Ser
|
|
NM_002693.3:c.3493G>T
MANE Select
|
NP_002684.1:p.Ala1165Ser
|
|