ENST00000403665.7:c.1304+387_1304+390del
MANE Select
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ENSP00000384957.2:n.1304+387_1304+390del
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ENST00000264692.8:c.1142+387_1142+390del
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ENSP00000264692.5:n.1142+387_1142+390del
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ENST00000403665.6:c.1304+387_1304+390del
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ENSP00000384957.2:n.1304+387_1304+390del
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NM_000128.3:c.1304+387_1304+390del , LRG_583t1:c.1304+387_1304+390del
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NP_000119.1:n.1304+387_1304+390del
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XM_005262821.2:c.1307+387_1307+390del
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XP_005262878.1:n.1307+387_1307+390del
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XM_005262822.2:c.1307+387_1307+390del
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XP_005262879.1:n.1307+387_1307+390del
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XM_005262823.2:c.1037+387_1037+390del
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XP_005262880.1:n.1037+387_1037+390del
|
|
XM_005262824.1:c.1307+387_1307+390del
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XP_005262881.1:n.1307+387_1307+390del
|
|
XM_006714137.1:c.1259+387_1259+390del
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XP_006714200.1:n.1259+387_1259+390del
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|
XR_938706.1:n.1712+387_1712+390del
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|
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XR_938707.1:n.1712+387_1712+390del
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|
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XM_005262821.4:c.1307+387_1307+390del
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XP_005262878.1:n.1307+387_1307+390del
|
|
XM_005262822.4:c.1307+387_1307+390del
|
XP_005262879.1:n.1307+387_1307+390del
|
|
XM_005262823.4:c.1037+387_1037+390del
|
XP_005262880.1:n.1037+387_1037+390del
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|
XM_006714137.3:c.1259+387_1259+390del
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XP_006714200.1:n.1259+387_1259+390del
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|
XR_001741172.2:n.1778+387_1778+390del
|
|
|
NM_000128.4:c.1304+387_1304+390del
MANE Select
|
NP_000119.1:n.1304+387_1304+390del
|
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