ENST00000325385.12:c.2022C>T
MANE Select
|
ENSP00000315569.7:p.Tyr674=
|
|
ENST00000273009.10:c.1582-9494C>T
|
ENSP00000273009.6:n.1582-9494C>T
|
|
ENST00000325385.11:c.2022C>T
|
ENSP00000315569.7:p.Tyr674=
|
|
ENST00000390005.9:c.*89C>T
|
ENSP00000374655.5:n.*89C>T
|
|
ENST00000409307.5:c.2022C>T
|
ENSP00000386799.1:p.Tyr674=
|
|
ENST00000424049.1:c.927C>T
|
ENSP00000415419.1:p.Tyr309=
|
|
ENST00000429283.2:n.1588C>T
|
|
|
ENST00000433430.5:c.3433C>T
|
ENSP00000391175.1:n.3433C>T
|
|
ENST00000445090.5:c.*1178C>T
|
ENSP00000388999.1:n.*1178C>T
|
|
NM_001257281.1:c.1582-9494C>T
|
NP_001244210.1:n.1582-9494C>T
|
|
NM_152383.4:c.2022C>T , LRG_534t1:c.2022C>T
|
NP_689596.4:p.Tyr674=
|
|
NR_046476.1:n.2225C>T
|
|
|
NR_046477.1:n.2204C>T
|
|
|
NM_001257281.2:c.1582-9494C>T
|
NP_001244210.1:n.1582-9494C>T
|
|
NM_152383.5:c.2022C>T
MANE Select
|
NP_689596.4:p.Tyr674=
|
|
NR_046476.2:n.2095C>T
|
|
|
NR_046477.2:n.2074C>T
|
|
|