ENST00000405460.9:c.9167T>A
MANE Select
|
ENSP00000384582.2:p.Leu3056Gln
|
|
ENST00000639431.1:c.265+36202T>A
|
ENSP00000491057.1:n.265+36202T>A
|
|
ENST00000639473.1:n.4626T>A
|
|
|
ENST00000640012.1:c.2974T>A
|
|
|
ENST00000640374.1:n.2311T>A
|
|
|
ENST00000640779.1:c.3896T>A
|
|
|
ENST00000405460.6:c.9167T>A
|
ENSP00000384582.2:p.Leu3056Gln
|
|
ENST00000509621.1:c.1864T>A
|
|
|
NM_032119.3:c.9167T>A
|
NP_115495.3:p.Leu3056Gln
|
|
NR_003149.1:n.9180T>A
|
|
|
XM_011543675.1:c.9164T>A
|
XP_011541977.1:p.Leu3055Gln
|
|
XM_011543676.1:c.9086T>A
|
XP_011541978.1:p.Leu3029Gln
|
|
XM_011543677.1:c.6470T>A
|
XP_011541979.1:p.Leu2157Gln
|
|
XM_011543678.1:c.9167T>A
|
XP_011541980.1:p.Leu3056Gln
|
|
XM_011543679.1:c.9167T>A
|
XP_011541981.1:p.Leu3056Gln
|
|
XR_948560.1:n.437-2A>T
|
|
|
NM_032119.4:c.9167T>A
MANE Select
|
NP_115495.3:p.Leu3056Gln
|
|
XM_017009963.2:c.9188T>A
|
XP_016865452.1:p.Leu3063Gln
|
|
XM_017009964.2:c.9185T>A
|
XP_016865453.1:p.Leu3062Gln
|
|
XM_017009965.1:c.9185T>A
|
XP_016865454.1:p.Leu3062Gln
|
|
XM_017009966.2:c.9107T>A
|
XP_016865455.1:p.Leu3036Gln
|
|
XM_017009967.1:c.9092T>A
|
XP_016865456.1:p.Leu3031Gln
|
|
XM_017009968.2:c.9188T>A
|
XP_016865457.1:p.Leu3063Gln
|
|
XM_017009969.2:c.9188T>A
|
XP_016865458.1:p.Leu3063Gln
|
|
XM_017009970.2:c.9188T>A
|
XP_016865459.1:p.Leu3063Gln
|
|
XM_017009971.2:c.9188T>A
|
XP_016865460.1:p.Leu3063Gln
|
|
XM_017009972.1:c.2306T>A
|
XP_016865461.1:p.Leu769Gln
|
|
XM_017009973.1:c.2285T>A
|
XP_016865462.1:p.Leu762Gln
|
|
XM_017009974.2:c.9188T>A
|
XP_016865463.1:p.Leu3063Gln
|
|
NR_003149.2:n.9183T>A
|
|
|