ENST00000378482.7:c.597+141G>A
MANE Select
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ENSP00000367743.2:n.597+141G>A
|
|
ENST00000286824.6:c.648+141G>A
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ENSP00000286824.6:n.648+141G>A
|
|
ENST00000378482.6:c.597+141G>A
|
ENSP00000367743.2:n.597+141G>A
|
|
ENST00000419600.3:n.541+141G>A
|
|
|
ENST00000465127.1:c.687+141G>A
|
ENSP00000417050.1:n.687+141G>A
|
|
ENST00000471410.5:c.*623+141G>A
|
ENSP00000419290.1:n.*623+141G>A
|
|
ENST00000475216.5:c.*590+141G>A
|
ENSP00000418586.1:n.*590+141G>A
|
|
NM_004615.3:c.597+141G>A
|
NP_004606.2:n.597+141G>A
|
|
NM_004615.4:c.597+141G>A
MANE Select
|
NP_004606.2:n.597+141G>A
|
|