ENST00000281928.9:c.6021G>T
MANE Select
|
ENSP00000281928.3:p.Val2007=
|
|
ENST00000548784.2:n.2235G>T
|
|
|
ENST00000648379.1:n.4389G>T
|
|
|
ENST00000648737.1:n.5785G>T
|
|
|
ENST00000648825.1:n.4206G>T
|
|
|
ENST00000648916.1:n.4032G>T
|
|
|
ENST00000649607.1:c.4205G>T
|
|
|
ENST00000649775.1:c.2510G>T
|
|
|
ENST00000650226.1:c.6057G>T
|
ENSP00000496981.1:p.Val2019=
|
|
ENST00000281928.7:c.6021G>T
|
ENSP00000281928.3:p.Val2007=
|
|
NM_015335.4:c.6021G>T
|
NP_056150.1:p.Val2007=
|
|
XM_011538080.1:c.6057G>T
|
XP_011536382.1:p.Val2019=
|
|
XM_011538081.1:c.6054G>T
|
XP_011536383.1:p.Val2018=
|
|
XM_011538082.1:c.6027G>T
|
XP_011536384.1:p.Val2009=
|
|
XM_011538080.2:c.6057G>T
|
XP_011536382.1:p.Val2019=
|
|
XM_011538081.2:c.6054G>T
|
XP_011536383.1:p.Val2018=
|
|
XM_011538082.2:c.6027G>T
|
XP_011536384.1:p.Val2009=
|
|
XM_017019090.1:c.6018G>T
|
XP_016874579.1:p.Val2006=
|
|
NM_015335.5:c.6021G>T
MANE Select
|
NP_056150.1:p.Val2007=
|
|