ENST00000636937.2:c.3609A>C
|
ENSP00000516154.1:p.Pro1203=
|
|
ENST00000268124.11:c.3609A>C
MANE Select
|
ENSP00000268124.5:p.Pro1203=
|
|
ENST00000530292.3:c.3309A>C
|
ENSP00000432885.2:n.3309A>C
|
|
ENST00000635986.2:c.*679A>C
|
ENSP00000490653.2:n.*679A>C
|
|
ENST00000636774.1:c.*2213A>C
|
ENSP00000489799.1:n.*2213A>C
|
|
ENST00000637238.1:c.2517A>C
|
ENSP00000490756.1:n.2517A>C
|
|
ENST00000637264.1:c.2621A>C
|
|
|
ENST00000666746.1:c.3186A>C
|
|
|
ENST00000672071.1:n.4811A>C
|
|
|
ENST00000672695.1:n.1388A>C
|
|
|
ENST00000672923.2:n.3609A>C
|
|
|
ENST00000268124.9:c.3609A>C
|
ENSP00000268124.5:p.Pro1203=
|
|
ENST00000442287.6:c.3609A>C
|
ENSP00000399851.2:p.Pro1203=
|
|
ENST00000526671.1:n.419A>C
|
|
|
ENST00000530292.2:c.792A>C
|
ENSP00000432885.1:n.792A>C
|
|
ENST00000631044.2:c.*3033A>C
|
ENSP00000486730.1:n.*3033A>C
|
|
NM_001126131.1:c.3609A>C
|
NP_001119603.1:p.Pro1203=
|
|
NM_002693.2:c.3609A>C
|
NP_002684.1:p.Pro1203=
|
|
NM_001126131.2:c.3609A>C
|
NP_001119603.1:p.Pro1203=
|
|
NM_002693.3:c.3609A>C
MANE Select
|
NP_002684.1:p.Pro1203=
|
|