ENST00000696154.2:n.1667G>A
|
|
|
ENST00000696154.1:c.*877G>A
|
ENSP00000512445.1:n.*877G>A
|
|
ENST00000696155.1:n.443G>A
|
|
|
ENST00000259089.9:c.*41G>A
MANE Select
|
ENSP00000259089.4:n.*41G>A
|
|
ENST00000645242.1:c.*41G>A
|
ENSP00000494690.1:n.*41G>A
|
|
ENST00000259089.8:c.*41G>A
|
ENSP00000259089.4:n.*41G>A
|
|
ENST00000526097.1:n.1499G>A
|
|
|
ENST00000529894.1:c.*41G>A
|
ENSP00000433663.1:n.*41G>A
|
|
NM_001715.2:c.*41G>A
|
NP_001706.2:n.*41G>A
|
|
XM_011543824.1:c.*41G>A
|
XP_011542126.1:n.*41G>A
|
|
XM_011543825.1:c.*41G>A
|
XP_011542127.1:n.*41G>A
|
|
XM_011543826.1:c.*41G>A
|
XP_011542128.1:n.*41G>A
|
|
XM_011543827.1:c.*41G>A
|
XP_011542129.1:n.*41G>A
|
|
NM_001330465.1:c.*41G>A
|
NP_001317394.1:n.*41G>A
|
|
XM_011543825.3:c.*41G>A
|
XP_011542127.1:n.*41G>A
|
|
NM_001715.3:c.*41G>A
MANE Select
|
NP_001706.2:n.*41G>A
|
|
NM_001330465.2:c.*41G>A
|
NP_001317394.1:n.*41G>A
|
|