ENST00000534624.6:c.1235T>C
MANE Select
|
ENSP00000432083.1:p.Val412Ala
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|
ENST00000227378.7:c.1235T>C
|
ENSP00000227378.3:p.Val412Ala
|
|
ENST00000453788.6:c.1235T>C
|
ENSP00000404372.2:p.Val412Ala
|
|
ENST00000524552.5:c.8T>C
|
ENSP00000435908.1:p.Val3Ala
|
|
ENST00000526110.5:c.1178T>C
|
ENSP00000433584.1:p.Val393Ala
|
|
ENST00000532091.1:n.982T>C
|
|
|
ENST00000532636.5:c.1235T>C
|
ENSP00000437125.1:p.Val412Ala
|
|
ENST00000533238.5:n.381-44T>C
|
|
|
ENST00000533540.5:c.797T>C
|
ENSP00000437189.1:p.Val266Ala
|
|
ENST00000534319.5:c.527T>C
|
ENSP00000433316.1:p.Val176Ala
|
|
ENST00000534624.5:c.1235T>C
|
ENSP00000432083.1:p.Val412Ala
|
|
NM_006597.5:c.1235T>C
|
NP_006588.1:p.Val412Ala
|
|
NM_153201.3:c.1235T>C
|
NP_694881.1:p.Val412Ala
|
|
XM_011542798.1:c.1235T>C
|
XP_011541100.1:p.Val412Ala
|
|
NM_006597.6:c.1235T>C
MANE Select
|
NP_006588.1:p.Val412Ala
|
|
NM_153201.4:c.1235T>C
|
NP_694881.1:p.Val412Ala
|
|