ENST00000281928.9:c.4339-134G>C
MANE Select
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ENSP00000281928.3:n.4339-134G>C
|
|
ENST00000549786.2:c.3767-134G>C
|
|
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ENST00000648379.1:n.2707-134G>C
|
|
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ENST00000648737.1:n.4103-134G>C
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|
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ENST00000648825.1:n.1079-134G>C
|
|
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ENST00000648916.1:n.2350-134G>C
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|
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ENST00000649146.1:n.935G>C
|
|
|
ENST00000649607.1:c.2523-134G>C
|
|
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ENST00000649775.1:c.836-134G>C
|
|
|
ENST00000650091.1:n.2315-134G>C
|
|
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ENST00000650226.1:c.4339-134G>C
|
ENSP00000496981.1:n.4339-134G>C
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|
ENST00000281928.7:c.4339-134G>C
|
ENSP00000281928.3:n.4339-134G>C
|
|
NM_015335.4:c.4339-134G>C
|
NP_056150.1:n.4339-134G>C
|
|
XM_011538080.1:c.4339-134G>C
|
XP_011536382.1:n.4339-134G>C
|
|
XM_011538081.1:c.4336-134G>C
|
XP_011536383.1:n.4336-134G>C
|
|
XM_011538082.1:c.4309-134G>C
|
XP_011536384.1:n.4309-134G>C
|
|
XM_011538080.2:c.4339-134G>C
|
XP_011536382.1:n.4339-134G>C
|
|
XM_011538081.2:c.4336-134G>C
|
XP_011536383.1:n.4336-134G>C
|
|
XM_011538082.2:c.4309-134G>C
|
XP_011536384.1:n.4309-134G>C
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|
XM_017019090.1:c.4336-134G>C
|
XP_016874579.1:n.4336-134G>C
|
|
NM_015335.5:c.4339-134G>C
MANE Select
|
NP_056150.1:n.4339-134G>C
|
|