ENST00000624552.4:c.14870G>C
|
ENSP00000485357.2:p.Gly4957Ala
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ENST00000683500.2:c.14927G>C
MANE Select
|
ENSP00000508292.2:p.Gly4976Ala
|
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ENST00000623487.1:n.3273G>C
|
|
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ENST00000624552.3:c.14867G>C
|
ENSP00000485357.1:p.Gly4956Ala
|
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NM_001291815.1:c.14927G>C
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NP_001278744.1:p.Gly4976Ala
|
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XM_011518465.1:c.14804G>C
|
XP_011516767.1:p.Gly4935Ala
|
|
XM_011518466.1:c.14795G>C
|
XP_011516768.1:p.Gly4932Ala
|
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XM_011518467.1:c.14750G>C
|
XP_011516769.1:p.Gly4917Ala
|
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NM_001291815.2:c.14927G>C
MANE Select
|
NP_001278744.1:p.Gly4976Ala
|
|
XM_011518465.2:c.14804G>C
|
XP_011516767.1:p.Gly4935Ala
|
|
XM_011518466.2:c.14795G>C
|
XP_011516768.1:p.Gly4932Ala
|
|
XM_011518467.2:c.14750G>C
|
XP_011516769.1:p.Gly4917Ala
|
|
XM_017014585.1:c.11708G>C
|
XP_016870074.1:p.Gly3903Ala
|
|
XM_017014586.1:c.7505G>C
|
XP_016870075.1:p.Gly2502Ala
|
|
XR_001746957.1:n.92+241C>G
|
|
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XR_001746958.1:n.92+241C>G
|
|
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