ENST00000405460.9:c.10872A>T
MANE Select
|
ENSP00000384582.2:p.Gln3624His
|
|
ENST00000425867.3:c.3A>T
|
ENSP00000392618.3:p.Gln1His
|
|
ENST00000639431.1:c.265+69484A>T
|
ENSP00000491057.1:n.265+69484A>T
|
|
ENST00000640374.1:n.4016A>T
|
|
|
ENST00000640464.1:n.1291A>T
|
|
|
ENST00000405460.6:c.10872A>T
|
ENSP00000384582.2:p.Gln3624His
|
|
ENST00000509621.1:c.3569A>T
|
|
|
NM_032119.3:c.10872A>T
|
NP_115495.3:p.Gln3624His
|
|
NR_003149.1:n.10885A>T
|
|
|
XM_011543675.1:c.10869A>T
|
XP_011541977.1:p.Gln3623His
|
|
XM_011543676.1:c.10791A>T
|
XP_011541978.1:p.Gln3597His
|
|
XM_011543677.1:c.8175A>T
|
XP_011541979.1:p.Gln2725His
|
|
XM_011543678.1:c.10872A>T
|
XP_011541980.1:p.Gln3624His
|
|
NM_032119.4:c.10872A>T
MANE Select
|
NP_115495.3:p.Gln3624His
|
|
XM_017009963.2:c.10893A>T
|
XP_016865452.1:p.Gln3631His
|
|
XM_017009964.2:c.10890A>T
|
XP_016865453.1:p.Gln3630His
|
|
XM_017009965.1:c.10890A>T
|
XP_016865454.1:p.Gln3630His
|
|
XM_017009966.2:c.10812A>T
|
XP_016865455.1:p.Gln3604His
|
|
XM_017009967.1:c.10797A>T
|
XP_016865456.1:p.Gln3599His
|
|
XM_017009968.2:c.10893A>T
|
XP_016865457.1:p.Gln3631His
|
|
XM_017009969.2:c.10893A>T
|
XP_016865458.1:p.Gln3631His
|
|
XM_017009970.2:c.10893A>T
|
XP_016865459.1:p.Gln3631His
|
|
XM_017009971.2:c.10893A>T
|
XP_016865460.1:p.Gln3631His
|
|
XM_017009972.1:c.4011A>T
|
XP_016865461.1:p.Gln1337His
|
|
XM_017009973.1:c.3990A>T
|
XP_016865462.1:p.Gln1330His
|
|
NR_003149.2:n.10888A>T
|
|
|