ENST00000295408.9:c.757+116_757+117insACC
MANE Select
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ENSP00000295408.4:n.757+116_757+117insACC
|
|
ENST00000295408.8:c.757+116_757+117insACC
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ENSP00000295408.4:n.757+116_757+117insACC
|
|
ENST00000409780.5:c.229+116_229+117insACC
|
ENSP00000387277.1:n.229+116_229+117insACC
|
|
ENST00000421804.6:c.757+116_757+117insACC
|
ENSP00000389152.2:n.757+116_757+117insACC
|
|
ENST00000439966.5:c.*230+116_*230+117insACC
|
ENSP00000402129.1:n.*230+116_*230+117insACC
|
|
ENST00000616902.4:c.-459+116_-459+117insACC
|
ENSP00000482824.1:n.-459+116_-459+117insACC
|
|
NM_006343.2:c.757+116_757+117insACC
|
NP_006334.2:n.757+116_757+117insACC
|
|
XM_005263565.3:c.757+116_757+117insACC
|
XP_005263622.1:n.757+116_757+117insACC
|
|
XM_005263568.3:c.757+116_757+117insACC
|
XP_005263625.1:n.757+116_757+117insACC
|
|
XM_011510490.1:c.568+116_568+117insACC
|
XP_011508792.1:n.568+116_568+117insACC
|
|
XM_005263565.4:c.757+116_757+117insACC
|
XP_005263622.1:n.757+116_757+117insACC
|
|
XM_005263568.4:c.757+116_757+117insACC
|
XP_005263625.1:n.757+116_757+117insACC
|
|
XM_011510490.3:c.568+116_568+117insACC
|
XP_011508792.1:n.568+116_568+117insACC
|
|
XM_017003164.1:c.568+116_568+117insACC
|
XP_016858653.1:n.568+116_568+117insACC
|
|
XM_017003165.2:c.-511+116_-511+117insACC
|
XP_016858654.1:n.-511+116_-511+117insACC
|
|
NM_006343.3:c.757+116_757+117insACC
MANE Select
|
NP_006334.2:n.757+116_757+117insACC
|
|