ENST00000696154.2:n.2077G>A
|
|
|
ENST00000696154.1:c.*1287G>A
|
ENSP00000512445.1:n.*1287G>A
|
|
ENST00000259089.9:c.*451G>A
MANE Select
|
ENSP00000259089.4:n.*451G>A
|
|
ENST00000645242.1:c.*451G>A
|
ENSP00000494690.1:n.*451G>A
|
|
ENST00000259089.8:c.*451G>A
|
ENSP00000259089.4:n.*451G>A
|
|
ENST00000526097.1:n.1909G>A
|
|
|
NM_001715.2:c.*451G>A
|
NP_001706.2:n.*451G>A
|
|
XM_011543824.1:c.*451G>A
|
XP_011542126.1:n.*451G>A
|
|
XM_011543825.1:c.*451G>A
|
XP_011542127.1:n.*451G>A
|
|
XM_011543826.1:c.*451G>A
|
XP_011542128.1:n.*451G>A
|
|
XM_011543827.1:c.*451G>A
|
XP_011542129.1:n.*451G>A
|
|
NM_001330465.1:c.*451G>A
|
NP_001317394.1:n.*451G>A
|
|
XM_011543825.3:c.*451G>A
|
XP_011542127.1:n.*451G>A
|
|
NM_001715.3:c.*451G>A
MANE Select
|
NP_001706.2:n.*451G>A
|
|
NM_001330465.2:c.*451G>A
|
NP_001317394.1:n.*451G>A
|
|