ENST00000261366.10:c.778T>C
MANE Select
|
ENSP00000261366.5:p.Tyr260His
|
|
ENST00000261366.9:c.778T>C
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ENSP00000261366.5:p.Tyr260His
|
|
ENST00000395354.1:c.778T>C
|
ENSP00000378761.1:p.Tyr260His
|
|
ENST00000460265.5:c.778T>C
|
ENSP00000486528.1:p.Tyr260His
|
|
ENST00000472034.5:n.511T>C
|
|
|
ENST00000504788.5:n.511T>C
|
|
|
NM_001198557.1:c.148T>C
|
NP_001185486.1:p.Tyr50His
|
|
NM_005573.3:c.778T>C
|
NP_005564.1:p.Tyr260His
|
|
XR_948250.1:n.1142T>C
|
|
|
NR_134488.1:n.1664T>C
|
|
|
NM_005573.4:c.778T>C
MANE Select
|
NP_005564.1:p.Tyr260His
|
|
NM_001198557.2:c.148T>C
|
NP_001185486.1:p.Tyr50His
|
|