|
ENST00000449880.7:c.4608C>T
(ITGB4)
|
ENSP00000400217.2:p.Cys1536=
|
|
|
ENST00000200181.8:c.4659C>T
(ITGB4)
MANE Select
|
ENSP00000200181.3:p.Cys1553=
|
|
|
ENST00000200181.7:c.4659C>T
(ITGB4)
|
ENSP00000200181.3:p.Cys1553=
|
|
|
ENST00000225614.6:c.*22+2233G>A
(GALK1)
|
ENSP00000225614.1:n.*22+2233G>A
|
|
|
ENST00000449880.6:c.4608C>T
(ITGB4)
|
ENSP00000400217.2:p.Cys1536=
|
|
|
ENST00000450894.7:c.4449C>T
(ITGB4)
|
ENSP00000405536.3:p.Cys1483=
|
|
|
ENST00000579662.5:c.4449C>T
(ITGB4)
|
ENSP00000463651.1:p.Cys1483=
|
|
|
ENST00000582629.1:c.266-1825C>T
(ITGB4)
|
ENSP00000463788.1:n.266-1825C>T
|
|
|
ENST00000583327.2:n.692C>T
(ITGB4)
|
|
|
|
ENST00000584939.1:c.199-628C>T
(ITGB4)
|
|
|
|
ENST00000589643.1:n.254+2233G>A
(GALK1)
|
|
|
|
NM_000213.3:c.4659C>T
(ITGB4)
|
NP_000204.3:p.Cys1553=
|
|
|
NM_001005619.1:c.4608C>T
(ITGB4)
|
NP_001005619.1:p.Cys1536=
|
|
|
NM_001005731.1:c.4449C>T
(ITGB4)
|
NP_001005731.1:p.Cys1483=
|
|
|
XM_005257309.2:c.4818C>T
(ITGB4)
|
XP_005257366.1:p.Cys1606=
|
|
|
XM_005257311.3:c.4818C>T
(ITGB4)
|
XP_005257368.1:p.Cys1606=
|
|
|
XM_005257312.2:c.4449C>T
(ITGB4)
|
XP_005257369.1:p.Cys1483=
|
|
|
XM_006721866.2:c.4923C>T
(ITGB4)
|
XP_006721929.1:p.Cys1641=
|
|
|
XM_006721867.2:c.4764C>T
(ITGB4)
|
XP_006721930.1:p.Cys1588=
|
|
|
XM_006721868.2:c.4713C>T
(ITGB4)
|
XP_006721931.1:p.Cys1571=
|
|
|
XM_006721870.2:c.4554C>T
(ITGB4)
|
XP_006721933.1:p.Cys1518=
|
|
|
XM_011524751.1:c.4664-628C>T
(ITGB4)
|
XP_011523053.1:n.4664-628C>T
|
|
|
XM_011524752.1:c.2763C>T
(ITGB4)
|
XP_011523054.1:p.Cys921=
|
|
|
NM_000213.4:c.4659C>T
(ITGB4)
|
NP_000204.3:p.Cys1553=
|
|
|
NM_001005731.2:c.4449C>T
(ITGB4)
|
NP_001005731.1:p.Cys1483=
|
|
|
NM_001321123.1:c.4449C>T
(ITGB4)
|
NP_001308052.1:p.Cys1483=
|
|
|
XM_005257311.4:c.4818C>T
(ITGB4)
|
XP_005257368.1:p.Cys1606=
|
|
|
XM_006721866.3:c.4923C>T
(ITGB4)
|
XP_006721929.1:p.Cys1641=
|
|
|
XM_006721867.3:c.4764C>T
(ITGB4)
|
XP_006721930.1:p.Cys1588=
|
|
|
XM_006721868.3:c.4713C>T
(ITGB4)
|
XP_006721931.1:p.Cys1571=
|
|
|
XM_006721870.3:c.4554C>T
(ITGB4)
|
XP_006721933.1:p.Cys1518=
|
|
|
XM_011524751.2:c.4664-628C>T
(ITGB4)
|
XP_011523053.1:n.4664-628C>T
|
|
|
XM_011524752.2:c.2763C>T
(ITGB4)
|
XP_011523054.1:p.Cys921=
|
|
|
NM_000213.5:c.4659C>T
(ITGB4)
MANE Select
|
NP_000204.3:p.Cys1553=
|
|
|
NM_001005731.3:c.4449C>T
(ITGB4)
|
NP_001005731.1:p.Cys1483=
|
|
|
NM_001321123.2:c.4449C>T
(ITGB4)
|
NP_001308052.1:p.Cys1483=
|
|
|
NM_001381985.1:c.*22+2233G>A
(GALK1)
|
NP_001368914.1:n.*22+2233G>A
|
|
