ENST00000311106.8:c.181-292G>C
MANE Select
|
ENSP00000308024.2:n.181-292G>C
|
|
ENST00000311106.7:c.181-292G>C
|
ENSP00000308024.2:n.181-292G>C
|
|
ENST00000508626.5:c.40-292G>C
|
ENSP00000421600.1:n.40-292G>C
|
|
ENST00000509190.1:c.181-292G>C
|
ENSP00000427294.1:n.181-292G>C
|
|
NM_000439.4:c.181-292G>C
|
NP_000430.3:n.181-292G>C
|
|
NM_001177875.1:c.40-292G>C
|
NP_001171346.1:n.40-292G>C
|
|
NR_130776.1:n.354+49957C>G
|
|
|
NM_000439.5:c.181-292G>C
MANE Select
|
NP_000430.3:n.181-292G>C
|
|
NM_001177875.2:c.40-292G>C
|
NP_001171346.1:n.40-292G>C
|
|