|
ENST00000684843.1:c.5809C>T
(MYH10)
|
ENSP00000509695.1:p.Arg1937Trp
|
|
|
ENST00000685418.1:c.*5076C>T
(MYH10)
|
ENSP00000510761.1:n.*5076C>T
|
|
|
ENST00000685631.1:n.6777C>T
(MYH10)
|
|
|
|
ENST00000686521.1:n.7404C>T
(MYH10)
|
|
|
|
ENST00000686654.1:c.5872C>T
(MYH10)
|
ENSP00000508862.1:p.Arg1958Trp
|
|
|
ENST00000687178.1:c.5806C>T
(MYH10)
|
ENSP00000509748.1:p.Arg1936Trp
|
|
|
ENST00000688497.1:c.*5154C>T
(MYH10)
|
ENSP00000509831.1:n.*5154C>T
|
|
|
ENST00000688902.1:c.5872C>T
(MYH10)
|
ENSP00000509091.1:p.Arg1958Trp
|
|
|
ENST00000691566.1:n.8842C>T
(MYH10)
|
|
|
|
ENST00000692526.1:c.5809C>T
(MYH10)
|
ENSP00000510471.1:p.Arg1937Trp
|
|
|
ENST00000693441.1:c.5872C>T
(MYH10)
|
ENSP00000509241.1:p.Arg1958Trp
|
|
|
ENST00000360416.8:c.5872C>T
(MYH10)
MANE Select
|
ENSP00000353590.4:p.Arg1958Trp
|
|
|
ENST00000269243.8:c.5779C>T
(MYH10)
|
ENSP00000269243.4:p.Arg1927Trp
|
|
|
ENST00000360416.7:c.5872C>T
(MYH10)
|
ENSP00000353590.3:p.Arg1958Trp
|
|
|
ENST00000379980.8:c.5806C>T
(MYH10)
|
ENSP00000369315.5:p.Arg1936Trp
|
|
|
ENST00000581679.1:c.418-13364G>A
(NDEL1)
|
|
|
|
NM_001256012.1:c.5872C>T
(MYH10)
|
NP_001242941.1:p.Arg1958Trp
|
|
|
NM_001256095.1:c.5806C>T
(MYH10)
|
NP_001243024.1:p.Arg1936Trp
|
|
|
NM_005964.3:c.5779C>T
(MYH10)
|
NP_005955.3:p.Arg1927Trp
|
|
|
XM_005256651.2:c.5872C>T
(MYH10)
|
XP_005256708.1:p.Arg1958Trp
|
|
|
XM_011523875.1:c.5962C>T
(MYH10)
|
XP_011522177.1:p.Arg1988Trp
|
|
|
XM_011523876.1:c.5959C>T
(MYH10)
|
XP_011522178.1:p.Arg1987Trp
|
|
|
XM_011523877.1:c.5932C>T
(MYH10)
|
XP_011522179.1:p.Arg1978Trp
|
|
|
XM_011523878.1:c.5899C>T
(MYH10)
|
XP_011522180.1:p.Arg1967Trp
|
|
|
XM_011523879.1:c.5896C>T
(MYH10)
|
XP_011522181.1:p.Arg1966Trp
|
|
|
XM_011523880.1:c.5869C>T
(MYH10)
|
XP_011522182.1:p.Arg1957Trp
|
|
|
XM_011523875.2:c.5962C>T
(MYH10)
|
XP_011522177.1:p.Arg1988Trp
|
|
|
XM_011523878.2:c.5899C>T
(MYH10)
|
XP_011522180.1:p.Arg1967Trp
|
|
|
XM_011523879.2:c.5896C>T
(MYH10)
|
XP_011522181.1:p.Arg1966Trp
|
|
|
XM_011523880.2:c.5869C>T
(MYH10)
|
XP_011522182.1:p.Arg1957Trp
|
|
|
XM_017024677.2:c.5809C>T
(MYH10)
|
XP_016880166.1:p.Arg1937Trp
|
|
|
XM_017024678.1:c.5809C>T
(MYH10)
|
XP_016880167.1:p.Arg1937Trp
|
|
|
XM_017024679.1:c.5809C>T
(MYH10)
|
XP_016880168.1:p.Arg1937Trp
|
|
|
XM_017024680.1:c.5806C>T
(MYH10)
|
XP_016880169.1:p.Arg1936Trp
|
|
|
XM_017024681.1:c.5779C>T
(MYH10)
|
XP_016880170.1:p.Arg1927Trp
|
|
|
XM_017024682.1:c.5779C>T
(MYH10)
|
XP_016880171.1:p.Arg1927Trp
|
|
|
NM_001256012.3:c.5872C>T
(MYH10)
MANE Select
|
NP_001242941.1:p.Arg1958Trp
|
|
|
NM_001375266.1:c.5809C>T
(MYH10)
|
NP_001362195.1:p.Arg1937Trp
|
|
|
NM_005964.4:c.5779C>T
(MYH10)
|
NP_005955.3:p.Arg1927Trp
|
|
|
NM_001256095.2:c.5806C>T
(MYH10)
|
NP_001243024.1:p.Arg1936Trp
|
|
|
NM_005964.5:c.5779C>T
(MYH10)
|
NP_005955.3:p.Arg1927Trp
|
|
