|
NM_032119.4:c.15987C>T
MANE Select
|
NP_115495.3:p.Tyr5329=
|
|
ENST00000405460.9:c.15987C>T
MANE Select
|
ENSP00000384582.2:p.Tyr5329=
|
|
NM_032119.3:c.15987C>T
|
NP_115495.3:p.Tyr5329=
|
|
NR_003149.1:n.16000C>T
|
|
|
NR_003149.2:n.16003C>T
|
|
|
ENST00000405460.6:c.15987C>T
|
ENSP00000384582.2:p.Tyr5329=
|
|
ENST00000425867.2:c.2970C>T
|
ENSP00000392618.2:p.Tyr990=
|
|
ENST00000425867.3:c.4941C>T
|
ENSP00000392618.3:p.Tyr1647=
|
|
ENST00000638510.1:n.3254C>T
|
|
|
ENST00000639431.1:c.265+135038C>T
|
ENSP00000491057.1:n.265+135038C>T
|
|
ENST00000640407.1:c.2397C>T
|
ENSP00000491425.1:p.Tyr799=
|
|
XM_011543675.1:c.15984C>T
|
XP_011541977.1:p.Tyr5328=
|
|
XM_011543676.1:c.15906C>T
|
XP_011541978.1:p.Tyr5302=
|
|
XM_011543677.1:c.13290C>T
|
XP_011541979.1:p.Tyr4430=
|
|
XM_017009963.2:c.16008C>T
|
XP_016865452.1:p.Tyr5336=
|
|
XM_017009964.2:c.16005C>T
|
XP_016865453.1:p.Tyr5335=
|
|
XM_017009965.1:c.16005C>T
|
XP_016865454.1:p.Tyr5335=
|
|
XM_017009966.2:c.15927C>T
|
XP_016865455.1:p.Tyr5309=
|
|
XM_017009967.1:c.15912C>T
|
XP_016865456.1:p.Tyr5304=
|
|
XM_017009968.2:c.15828C>T
|
XP_016865457.1:p.Tyr5276=
|
|
XM_017009969.2:c.16008C>T
|
XP_016865458.1:p.Tyr5336=
|
|
XM_017009972.1:c.9126C>T
|
XP_016865461.1:p.Tyr3042=
|
|
XM_017009973.1:c.9105C>T
|
XP_016865462.1:p.Tyr3035=
|