ENST00000650516.2:c.913G>T
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ENSP00000498052.2:p.Gly305Ter
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ENST00000343257.7:c.913G>T
MANE Select
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ENSP00000339867.2:p.Gly305Ter
|
|
ENST00000432192.6:c.737G>T
|
|
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ENST00000455478.6:c.501G>T
|
ENSP00000400027.2:n.501G>T
|
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ENST00000650516.1:c.913G>T
|
ENSP00000498052.1:p.Gly305Ter
|
|
ENST00000343257.6:c.913G>T
|
ENSP00000339867.2:p.Gly305Ter
|
|
ENST00000432192.5:c.427G>T
|
|
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ENST00000455478.5:c.505G>T
|
|
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ENST00000495612.1:n.214G>T
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NM_000083.2:c.913G>T
|
NP_000074.2:p.Gly305Ter
|
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NR_046453.1:n.1003G>T
|
|
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XM_011515781.1:c.913G>T
|
XP_011514083.1:p.Gly305Ter
|
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XM_017011739.1:c.463G>T
|
XP_016867228.1:p.Gly155Ter
|
|
XM_017011740.1:c.463G>T
|
XP_016867229.1:p.Gly155Ter
|
|
NM_000083.3:c.913G>T
MANE Select
|
NP_000074.3:p.Gly305Ter
|
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NR_046453.2:n.1018G>T
|
|
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