ENST00000449880.7:c.5281G>C
(ITGB4)
|
ENSP00000400217.2:p.Gly1761Arg
|
|
ENST00000200181.8:c.5332G>C
(ITGB4)
MANE Select
|
ENSP00000200181.3:p.Gly1778Arg
|
|
ENST00000200181.7:c.5332G>C
(ITGB4)
|
ENSP00000200181.3:p.Gly1778Arg
|
|
ENST00000225614.6:c.*22+616C>G
(GALK1)
|
ENSP00000225614.1:n.*22+616C>G
|
|
ENST00000449880.6:c.5281G>C
(ITGB4)
|
ENSP00000400217.2:p.Gly1761Arg
|
|
ENST00000450894.7:c.5122G>C
(ITGB4)
|
ENSP00000405536.3:p.Gly1708Arg
|
|
ENST00000578318.1:c.288G>C
(ITGB4)
|
|
|
ENST00000579662.5:c.5122G>C
(ITGB4)
|
ENSP00000463651.1:p.Gly1708Arg
|
|
ENST00000582629.1:c.266-208G>C
(ITGB4)
|
ENSP00000463788.1:n.266-208G>C
|
|
ENST00000589643.1:n.254+616C>G
(GALK1)
|
|
|
NM_000213.3:c.5332G>C
(ITGB4)
|
NP_000204.3:p.Gly1778Arg
|
|
NM_001005619.1:c.5281G>C
(ITGB4)
|
NP_001005619.1:p.Gly1761Arg
|
|
NM_001005731.1:c.5122G>C
(ITGB4)
|
NP_001005731.1:p.Gly1708Arg
|
|
XM_005257309.2:c.5491G>C
(ITGB4)
|
XP_005257366.1:p.Gly1831Arg
|
|
XM_005257311.3:c.5491G>C
(ITGB4)
|
XP_005257368.1:p.Gly1831Arg
|
|
XM_005257312.2:c.5122G>C
(ITGB4)
|
XP_005257369.1:p.Gly1708Arg
|
|
XM_006721866.2:c.5596G>C
(ITGB4)
|
XP_006721929.1:p.Gly1866Arg
|
|
XM_006721867.2:c.5437G>C
(ITGB4)
|
XP_006721930.1:p.Gly1813Arg
|
|
XM_006721868.2:c.5386G>C
(ITGB4)
|
XP_006721931.1:p.Gly1796Arg
|
|
XM_006721870.2:c.5227G>C
(ITGB4)
|
XP_006721933.1:p.Gly1743Arg
|
|
XM_011524751.1:c.5287G>C
(ITGB4)
|
XP_011523053.1:p.Gly1763Arg
|
|
XM_011524752.1:c.3436G>C
(ITGB4)
|
XP_011523054.1:p.Gly1146Arg
|
|
NM_000213.4:c.5332G>C
(ITGB4)
|
NP_000204.3:p.Gly1778Arg
|
|
NM_001005731.2:c.5122G>C
(ITGB4)
|
NP_001005731.1:p.Gly1708Arg
|
|
NM_001321123.1:c.5122G>C
(ITGB4)
|
NP_001308052.1:p.Gly1708Arg
|
|
XM_005257311.4:c.5491G>C
(ITGB4)
|
XP_005257368.1:p.Gly1831Arg
|
|
XM_006721866.3:c.5596G>C
(ITGB4)
|
XP_006721929.1:p.Gly1866Arg
|
|
XM_006721867.3:c.5437G>C
(ITGB4)
|
XP_006721930.1:p.Gly1813Arg
|
|
XM_006721868.3:c.5386G>C
(ITGB4)
|
XP_006721931.1:p.Gly1796Arg
|
|
XM_006721870.3:c.5227G>C
(ITGB4)
|
XP_006721933.1:p.Gly1743Arg
|
|
XM_011524751.2:c.5287G>C
(ITGB4)
|
XP_011523053.1:p.Gly1763Arg
|
|
XM_011524752.2:c.3436G>C
(ITGB4)
|
XP_011523054.1:p.Gly1146Arg
|
|
NM_000213.5:c.5332G>C
(ITGB4)
MANE Select
|
NP_000204.3:p.Gly1778Arg
|
|
NM_001005731.3:c.5122G>C
(ITGB4)
|
NP_001005731.1:p.Gly1708Arg
|
|
NM_001321123.2:c.5122G>C
(ITGB4)
|
NP_001308052.1:p.Gly1708Arg
|
|
NM_001381985.1:c.*22+616C>G
(GALK1)
|
NP_001368914.1:n.*22+616C>G
|
|