ENST00000281928.9:c.6330C>T
MANE Select
|
ENSP00000281928.3:p.Pro2110=
|
|
ENST00000548784.2:n.2544C>T
|
|
|
ENST00000648379.1:n.4698C>T
|
|
|
ENST00000648737.1:n.6094C>T
|
|
|
ENST00000648762.1:n.1020C>T
|
|
|
ENST00000648825.1:n.4515C>T
|
|
|
ENST00000648916.1:n.4341C>T
|
|
|
ENST00000649607.1:c.4514C>T
|
|
|
ENST00000649775.1:c.2661C>T
|
|
|
ENST00000650226.1:c.6366C>T
|
ENSP00000496981.1:p.Pro2122=
|
|
ENST00000281928.7:c.6330C>T
|
ENSP00000281928.3:p.Pro2110=
|
|
NM_015335.4:c.6330C>T
|
NP_056150.1:p.Pro2110=
|
|
XM_011538080.1:c.6366C>T
|
XP_011536382.1:p.Pro2122=
|
|
XM_011538081.1:c.6363C>T
|
XP_011536383.1:p.Pro2121=
|
|
XM_011538082.1:c.6336C>T
|
XP_011536384.1:p.Pro2112=
|
|
XM_011538080.2:c.6366C>T
|
XP_011536382.1:p.Pro2122=
|
|
XM_011538081.2:c.6363C>T
|
XP_011536383.1:p.Pro2121=
|
|
XM_011538082.2:c.6336C>T
|
XP_011536384.1:p.Pro2112=
|
|
XM_017019090.1:c.6327C>T
|
XP_016874579.1:p.Pro2109=
|
|
NM_015335.5:c.6330C>T
MANE Select
|
NP_056150.1:p.Pro2110=
|
|