ENST00000264613.11:c.1869G>C
MANE Select
|
ENSP00000264613.6:p.Met623Ile
|
|
ENST00000264613.10:c.1869G>C
|
ENSP00000264613.6:p.Met623Ile
|
|
ENST00000462336.5:n.243G>C
|
|
|
ENST00000481169.5:c.1865-1282G>C
|
ENSP00000418773.1:n.1865-1282G>C
|
|
ENST00000489736.5:n.1094G>C
|
|
|
ENST00000490639.5:n.1901G>C
|
|
|
ENST00000494544.1:c.1218G>C
|
ENSP00000420545.1:p.Met406Ile
|
|
ENST00000497902.5:n.50G>C
|
|
|
NM_000096.3:c.1869G>C
|
NP_000087.1:p.Met623Ile
|
|
NR_046371.1:n.2118-1282G>C
|
|
|
XM_006713499.2:c.1869G>C
|
XP_006713562.1:p.Met623Ile
|
|
XM_006713500.2:c.1869G>C
|
XP_006713563.1:p.Met623Ile
|
|
XM_006713501.2:c.1869G>C
|
XP_006713564.1:p.Met623Ile
|
|
XM_006713502.2:c.1869G>C
|
XP_006713565.1:p.Met623Ile
|
|
XM_011512435.1:c.1869G>C
|
XP_011510737.1:p.Met623Ile
|
|
XR_427361.2:n.2127G>C
|
|
|
XM_006713499.3:c.1869G>C
|
XP_006713562.1:p.Met623Ile
|
|
XM_006713500.4:c.1869G>C
|
XP_006713563.1:p.Met623Ile
|
|
XM_006713501.3:c.1869G>C
|
XP_006713564.1:p.Met623Ile
|
|
XM_011512435.2:c.1869G>C
|
XP_011510737.1:p.Met623Ile
|
|
XM_017005734.2:c.1869G>C
|
XP_016861223.1:p.Met623Ile
|
|
XM_017005735.2:c.1869G>C
|
XP_016861224.1:p.Met623Ile
|
|
XR_427361.3:n.2085G>C
|
|
|
NM_000096.4:c.1869G>C
MANE Select
|
NP_000087.2:p.Met623Ile
|
|
NR_046371.2:n.1902-1282G>C
|
|
|