ENST00000281928.9:c.4955+228A>C
MANE Select
|
ENSP00000281928.3:n.4955+228A>C
|
|
ENST00000549786.2:c.4383+228A>C
|
|
|
ENST00000648379.1:n.3323+228A>C
|
|
|
ENST00000648737.1:n.4719+228A>C
|
|
|
ENST00000648825.1:n.1695+228A>C
|
|
|
ENST00000648916.1:n.2966+228A>C
|
|
|
ENST00000649146.1:n.1913A>C
|
|
|
ENST00000649607.1:c.3139+228A>C
|
|
|
ENST00000649775.1:c.1452+228A>C
|
|
|
ENST00000650226.1:c.4955+228A>C
|
ENSP00000496981.1:n.4955+228A>C
|
|
ENST00000281928.7:c.4955+228A>C
|
ENSP00000281928.3:n.4955+228A>C
|
|
ENST00000549786.1:c.319+228A>C
|
|
|
NM_015335.4:c.4955+228A>C
|
NP_056150.1:n.4955+228A>C
|
|
XM_011538080.1:c.4955+228A>C
|
XP_011536382.1:n.4955+228A>C
|
|
XM_011538081.1:c.4952+228A>C
|
XP_011536383.1:n.4952+228A>C
|
|
XM_011538082.1:c.4925+228A>C
|
XP_011536384.1:n.4925+228A>C
|
|
XM_011538080.2:c.4955+228A>C
|
XP_011536382.1:n.4955+228A>C
|
|
XM_011538081.2:c.4952+228A>C
|
XP_011536383.1:n.4952+228A>C
|
|
XM_011538082.2:c.4925+228A>C
|
XP_011536384.1:n.4925+228A>C
|
|
XM_017019090.1:c.4952+228A>C
|
XP_016874579.1:n.4952+228A>C
|
|
NM_015335.5:c.4955+228A>C
MANE Select
|
NP_056150.1:n.4955+228A>C
|
|