ENST00000405460.9:c.9407C>A
MANE Select
|
ENSP00000384582.2:p.Ser3136Tyr
|
|
ENST00000639431.1:c.265+40480C>A
|
ENSP00000491057.1:n.265+40480C>A
|
|
ENST00000639473.1:n.4866C>A
|
|
|
ENST00000640012.1:c.3214C>A
|
|
|
ENST00000640374.1:n.2551C>A
|
|
|
ENST00000640779.1:c.4136C>A
|
|
|
ENST00000405460.6:c.9407C>A
|
ENSP00000384582.2:p.Ser3136Tyr
|
|
ENST00000509621.1:c.2104C>A
|
|
|
NM_032119.3:c.9407C>A
|
NP_115495.3:p.Ser3136Tyr
|
|
NR_003149.1:n.9420C>A
|
|
|
XM_011543675.1:c.9404C>A
|
XP_011541977.1:p.Ser3135Tyr
|
|
XM_011543676.1:c.9326C>A
|
XP_011541978.1:p.Ser3109Tyr
|
|
XM_011543677.1:c.6710C>A
|
XP_011541979.1:p.Ser2237Tyr
|
|
XM_011543678.1:c.9407C>A
|
XP_011541980.1:p.Ser3136Tyr
|
|
XM_011543679.1:c.9407C>A
|
XP_011541981.1:p.Ser3136Tyr
|
|
XR_948560.1:n.272-880G>T
|
|
|
NM_032119.4:c.9407C>A
MANE Select
|
NP_115495.3:p.Ser3136Tyr
|
|
XM_017009963.2:c.9428C>A
|
XP_016865452.1:p.Ser3143Tyr
|
|
XM_017009964.2:c.9425C>A
|
XP_016865453.1:p.Ser3142Tyr
|
|
XM_017009965.1:c.9425C>A
|
XP_016865454.1:p.Ser3142Tyr
|
|
XM_017009966.2:c.9347C>A
|
XP_016865455.1:p.Ser3116Tyr
|
|
XM_017009967.1:c.9332C>A
|
XP_016865456.1:p.Ser3111Tyr
|
|
XM_017009968.2:c.9428C>A
|
XP_016865457.1:p.Ser3143Tyr
|
|
XM_017009969.2:c.9428C>A
|
XP_016865458.1:p.Ser3143Tyr
|
|
XM_017009970.2:c.9428C>A
|
XP_016865459.1:p.Ser3143Tyr
|
|
XM_017009971.2:c.9428C>A
|
XP_016865460.1:p.Ser3143Tyr
|
|
XM_017009972.1:c.2546C>A
|
XP_016865461.1:p.Ser849Tyr
|
|
XM_017009973.1:c.2525C>A
|
XP_016865462.1:p.Ser842Tyr
|
|
XM_017009974.2:c.9428C>A
|
XP_016865463.1:p.Ser3143Tyr
|
|
XR_001742802.1:n.2523-880G>T
|
|
|
NR_003149.2:n.9423C>A
|
|
|