ENST00000296684.10:c.199G>T
MANE Select
|
ENSP00000296684.5:p.Val67Phe
|
|
ENST00000296684.9:c.199G>T
|
ENSP00000296684.5:p.Val67Phe
|
|
ENST00000502423.5:c.*66G>T
|
ENSP00000422177.1:n.*66G>T
|
|
ENST00000506765.1:c.187G>T
|
ENSP00000424570.1:p.Val63Phe
|
|
ENST00000506974.5:c.371G>T
|
ENSP00000425967.1:p.Ser124Ile
|
|
ENST00000507026.5:c.*173G>T
|
ENSP00000424993.1:n.*173G>T
|
|
ENST00000509443.1:n.60G>T
|
|
|
NM_002495.2:c.199G>T
|
NP_002486.1:p.Val67Phe
|
|
XM_005248525.3:c.199G>T
|
XP_005248582.1:p.Val67Phe
|
|
XM_011543415.1:c.25G>T
|
XP_011541717.1:p.Val9Phe
|
|
NM_001318051.1:c.199G>T
|
NP_001304980.1:p.Val67Phe
|
|
NM_002495.3:c.199G>T
|
NP_002486.1:p.Val67Phe
|
|
NR_134473.1:n.401G>T
|
|
|
NR_134474.1:n.318G>T
|
|
|
NR_134475.1:n.353G>T
|
|
|
NM_002495.4:c.199G>T
MANE Select
|
NP_002486.1:p.Val67Phe
|
|
NM_001318051.2:c.199G>T
|
NP_001304980.1:p.Val67Phe
|
|
NR_134473.2:n.395G>T
|
|
|
NR_134474.2:n.312G>T
|
|
|
NR_134475.2:n.347G>T
|
|
|