ENST00000298910.12:c.7094T>A
MANE Select
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ENSP00000298910.7:p.Ile2365Asn
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ENST00000636518.1:c.891T>A
|
|
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ENST00000679360.1:c.*6003T>A
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ENSP00000505368.1:n.*6003T>A
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ENST00000679532.1:c.2868T>A
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|
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ENST00000679683.1:c.884T>A
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|
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ENST00000680018.1:c.2539T>A
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ENSP00000505347.1:n.2539T>A
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|
ENST00000680422.1:c.4181T>A
|
|
|
ENST00000680425.1:c.2261T>A
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ENSP00000506459.1:n.2261T>A
|
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ENST00000680453.1:c.2551T>A
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ENST00000680790.1:c.6839T>A
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ENSP00000505335.1:p.Ile2280Asn
|
|
ENST00000681136.1:n.3078T>A
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|
|
ENST00000681696.1:c.2777T>A
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ENSP00000505871.1:p.Ile926Asn
|
|
ENST00000681773.1:n.301T>A
|
|
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ENST00000298910.11:c.7094T>A
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ENSP00000298910.7:p.Ile2365Asn
|
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ENST00000430804.5:c.4390T>A
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|
|
ENST00000479187.5:n.3775T>A
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NM_198578.3:c.7094T>A
|
NP_940980.3:p.Ile2365Asn
|
|
XM_005268629.2:c.7094T>A
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XP_005268686.1:p.Ile2365Asn
|
|
XM_011537877.1:c.7094T>A
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XP_011536179.1:p.Ile2365Asn
|
|
XM_011537879.1:c.5891T>A
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XP_011536181.1:p.Ile1964Asn
|
|
XR_944868.1:n.485-8640A>T
|
|
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XM_005268629.4:c.7094T>A
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XP_005268686.1:p.Ile2365Asn
|
|
XM_011537877.3:c.7094T>A
|
XP_011536179.1:p.Ile2365Asn
|
|
XM_017018787.1:c.4010T>A
|
XP_016874276.1:p.Ile1337Asn
|
|
XM_017018788.2:c.3356T>A
|
XP_016874277.1:p.Ile1119Asn
|
|
XM_024448833.1:c.5891T>A
|
XP_024304601.1:p.Ile1964Asn
|
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XR_944868.2:n.485-8640A>T
|
|
|
NM_198578.4:c.7094T>A
MANE Select
|
NP_940980.4:p.Ile2365Asn
|
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