ENST00000296684.10:c.386G>T
MANE Select
|
ENSP00000296684.5:p.Ser129Ile
|
|
ENST00000296684.9:c.386G>T
|
ENSP00000296684.5:p.Ser129Ile
|
|
ENST00000502423.5:c.*253G>T
|
ENSP00000422177.1:n.*253G>T
|
|
ENST00000506765.1:c.338+12181G>T
|
ENSP00000424570.1:n.338+12181G>T
|
|
ENST00000506974.5:c.*162G>T
|
ENSP00000425967.1:n.*162G>T
|
|
ENST00000507026.5:c.*360G>T
|
ENSP00000424993.1:n.*360G>T
|
|
ENST00000509443.1:n.247G>T
|
|
|
NM_002495.2:c.386G>T
|
NP_002486.1:p.Ser129Ile
|
|
XM_005248525.3:c.350+12181G>T
|
XP_005248582.1:n.350+12181G>T
|
|
XM_011543415.1:c.212G>T
|
XP_011541717.1:p.Ser71Ile
|
|
NM_001318051.1:c.350+12181G>T
|
NP_001304980.1:n.350+12181G>T
|
|
NM_002495.3:c.386G>T
|
NP_002486.1:p.Ser129Ile
|
|
NR_134473.1:n.588G>T
|
|
|
NR_134474.1:n.505G>T
|
|
|
NR_134475.1:n.540G>T
|
|
|
NM_002495.4:c.386G>T
MANE Select
|
NP_002486.1:p.Ser129Ile
|
|
NM_001318051.2:c.350+12181G>T
|
NP_001304980.1:n.350+12181G>T
|
|
NR_134473.2:n.582G>T
|
|
|
NR_134474.2:n.499G>T
|
|
|
NR_134475.2:n.534G>T
|
|
|