|
NM_032119.4:c.16375C>T
MANE Select
|
NP_115495.3:p.Gln5459Ter
|
|
ENST00000405460.9:c.16375C>T
MANE Select
|
ENSP00000384582.2:p.Gln5459Ter
|
|
NM_032119.3:c.16375C>T
|
NP_115495.3:p.Gln5459Ter
|
|
NR_003149.1:n.16388C>T
|
|
|
NR_003149.2:n.16391C>T
|
|
|
ENST00000405460.6:c.16375C>T
|
ENSP00000384582.2:p.Gln5459Ter
|
|
ENST00000425867.2:c.3358C>T
|
ENSP00000392618.2:p.Gln1120Ter
|
|
ENST00000425867.3:c.5329C>T
|
ENSP00000392618.3:p.Gln1777Ter
|
|
ENST00000638510.1:n.3642C>T
|
|
|
ENST00000639431.1:c.265+152741C>T
|
ENSP00000491057.1:n.265+152741C>T
|
|
ENST00000640061.1:n.128+6768C>T
|
|
|
ENST00000640407.1:c.2824C>T
|
ENSP00000491425.1:n.2824C>T
|
|
XM_011543675.1:c.16372C>T
|
XP_011541977.1:p.Gln5458Ter
|
|
XM_011543676.1:c.16294C>T
|
XP_011541978.1:p.Gln5432Ter
|
|
XM_011543677.1:c.13678C>T
|
XP_011541979.1:p.Gln4560Ter
|
|
XM_017009963.2:c.16396C>T
|
XP_016865452.1:p.Gln5466Ter
|
|
XM_017009964.2:c.16393C>T
|
XP_016865453.1:p.Gln5465Ter
|
|
XM_017009965.1:c.16393C>T
|
XP_016865454.1:p.Gln5465Ter
|
|
XM_017009966.2:c.16315C>T
|
XP_016865455.1:p.Gln5439Ter
|
|
XM_017009967.1:c.16300C>T
|
XP_016865456.1:p.Gln5434Ter
|
|
XM_017009968.2:c.16216C>T
|
XP_016865457.1:p.Gln5406Ter
|
|
XM_017009969.2:c.16396C>T
|
XP_016865458.1:p.Gln5466Ter
|
|
XM_017009972.1:c.9514C>T
|
XP_016865461.1:p.Gln3172Ter
|
|
XM_017009973.1:c.9493C>T
|
XP_016865462.1:p.Gln3165Ter
|