ENST00000405460.9:c.9367G>T
MANE Select
|
ENSP00000384582.2:p.Glu3123Ter
|
|
ENST00000639431.1:c.265+40440G>T
|
ENSP00000491057.1:n.265+40440G>T
|
|
ENST00000639473.1:n.4826G>T
|
|
|
ENST00000640012.1:c.3174G>T
|
|
|
ENST00000640374.1:n.2511G>T
|
|
|
ENST00000640779.1:c.4096G>T
|
|
|
ENST00000405460.6:c.9367G>T
|
ENSP00000384582.2:p.Glu3123Ter
|
|
ENST00000509621.1:c.2064G>T
|
|
|
NM_032119.3:c.9367G>T
|
NP_115495.3:p.Glu3123Ter
|
|
NR_003149.1:n.9380G>T
|
|
|
XM_011543675.1:c.9364G>T
|
XP_011541977.1:p.Glu3122Ter
|
|
XM_011543676.1:c.9286G>T
|
XP_011541978.1:p.Glu3096Ter
|
|
XM_011543677.1:c.6670G>T
|
XP_011541979.1:p.Glu2224Ter
|
|
XM_011543678.1:c.9367G>T
|
XP_011541980.1:p.Glu3123Ter
|
|
XM_011543679.1:c.9367G>T
|
XP_011541981.1:p.Glu3123Ter
|
|
XR_948560.1:n.272-840C>A
|
|
|
NM_032119.4:c.9367G>T
MANE Select
|
NP_115495.3:p.Glu3123Ter
|
|
XM_017009963.2:c.9388G>T
|
XP_016865452.1:p.Glu3130Ter
|
|
XM_017009964.2:c.9385G>T
|
XP_016865453.1:p.Glu3129Ter
|
|
XM_017009965.1:c.9385G>T
|
XP_016865454.1:p.Glu3129Ter
|
|
XM_017009966.2:c.9307G>T
|
XP_016865455.1:p.Glu3103Ter
|
|
XM_017009967.1:c.9292G>T
|
XP_016865456.1:p.Glu3098Ter
|
|
XM_017009968.2:c.9388G>T
|
XP_016865457.1:p.Glu3130Ter
|
|
XM_017009969.2:c.9388G>T
|
XP_016865458.1:p.Glu3130Ter
|
|
XM_017009970.2:c.9388G>T
|
XP_016865459.1:p.Glu3130Ter
|
|
XM_017009971.2:c.9388G>T
|
XP_016865460.1:p.Glu3130Ter
|
|
XM_017009972.1:c.2506G>T
|
XP_016865461.1:p.Glu836Ter
|
|
XM_017009973.1:c.2485G>T
|
XP_016865462.1:p.Glu829Ter
|
|
XM_017009974.2:c.9388G>T
|
XP_016865463.1:p.Glu3130Ter
|
|
XR_001742802.1:n.2523-840C>A
|
|
|
NR_003149.2:n.9383G>T
|
|
|