ENST00000298910.12:c.6455T>G
MANE Select
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ENSP00000298910.7:p.Val2152Gly
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ENST00000636518.1:c.252T>G
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ENST00000679360.1:c.*5364T>G
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ENSP00000505368.1:n.*5364T>G
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ENST00000679532.1:c.2229T>G
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ENST00000679683.1:c.245T>G
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|
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ENST00000680018.1:c.1900T>G
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ENSP00000505347.1:n.1900T>G
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ENST00000680422.1:c.2100T>G
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|
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ENST00000680425.1:c.1622T>G
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ENSP00000506459.1:n.1622T>G
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|
ENST00000680453.1:c.1912T>G
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ENST00000680790.1:c.6200T>G
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ENSP00000505335.1:p.Val2067Gly
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ENST00000681136.1:n.2439T>G
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|
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ENST00000681696.1:c.2138T>G
|
ENSP00000505871.1:p.Val713Gly
|
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ENST00000298910.11:c.6455T>G
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ENSP00000298910.7:p.Val2152Gly
|
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ENST00000430804.5:c.3751T>G
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|
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ENST00000479187.5:n.3136T>G
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|
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NM_198578.3:c.6455T>G
|
NP_940980.3:p.Val2152Gly
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XM_005268629.2:c.6455T>G
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XP_005268686.1:p.Val2152Gly
|
|
XM_011537877.1:c.6455T>G
|
XP_011536179.1:p.Val2152Gly
|
|
XM_011537878.1:c.6455T>G
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XP_011536180.1:p.Val2152Gly
|
|
XM_011537879.1:c.5252T>G
|
XP_011536181.1:p.Val1751Gly
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XM_005268629.4:c.6455T>G
|
XP_005268686.1:p.Val2152Gly
|
|
XM_011537877.3:c.6455T>G
|
XP_011536179.1:p.Val2152Gly
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XM_017018787.1:c.3371T>G
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XP_016874276.1:p.Val1124Gly
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XM_017018788.2:c.2717T>G
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XP_016874277.1:p.Val906Gly
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XM_024448833.1:c.5252T>G
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XP_024304601.1:p.Val1751Gly
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|
NM_198578.4:c.6455T>G
MANE Select
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NP_940980.4:p.Val2152Gly
|
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