ENST00000647814.1:c.2702T>G
MANE Select
|
ENSP00000497274.1:p.Ile901Arg
|
|
ENST00000370449.8:c.2702T>G
|
ENSP00000359478.4:p.Ile901Arg
|
|
NM_000392.4:c.2702T>G
|
NP_000383.1:p.Ile901Arg
|
|
XM_006717630.2:c.2006T>G
|
XP_006717693.1:p.Ile669Arg
|
|
XM_006717631.2:c.*129T>G
|
XP_006717694.1:n.*129T>G
|
|
XM_011539291.1:c.2702T>G
|
XP_011537593.1:p.Ile901Arg
|
|
XR_945604.1:n.2891T>G
|
|
|
XR_945605.1:n.2893T>G
|
|
|
NM_000392.5:c.2702T>G
MANE Select
|
NP_000383.2:p.Ile901Arg
|
|
XM_006717630.3:c.2006T>G
|
XP_006717693.1:p.Ile669Arg
|
|
XM_006717631.4:c.*129T>G
|
XP_006717694.1:n.*129T>G
|
|
XM_011539291.3:c.2702T>G
|
XP_011537593.1:p.Ile901Arg
|
|
XR_945604.3:n.2945T>G
|
|
|
XR_945605.3:n.2945T>G
|
|
|