ENST00000706989.1:c.2525T>C
|
ENSP00000516702.1:p.Val842Ala
|
|
ENST00000359125.7:c.2471T>C
MANE Select
|
ENSP00000352035.2:p.Val824Ala
|
|
ENST00000637193.1:c.1868T>C
|
ENSP00000490734.1:p.Val623Ala
|
|
ENST00000344462.8:c.2378T>C
|
ENSP00000339611.4:p.Val793Ala
|
|
ENST00000357249.6:c.2039T>C
|
ENSP00000349789.3:p.Val680Ala
|
|
ENST00000359125.6:c.2471T>C
|
ENSP00000352035.2:p.Val824Ala
|
|
ENST00000360480.7:c.2387T>C
|
ENSP00000353668.3:p.Val796Ala
|
|
ENST00000370224.5:c.2241+254T>C
|
ENSP00000359244.2:n.2241+254T>C
|
|
ENST00000625514.2:c.2205+254T>C
|
ENSP00000486040.1:n.2205+254T>C
|
|
ENST00000626839.2:c.2417T>C
|
ENSP00000486706.1:p.Val806Ala
|
|
ENST00000629241.2:c.2133+254T>C
|
ENSP00000487142.1:n.2133+254T>C
|
|
ENST00000629676.2:c.1680-5949T>C
|
ENSP00000486194.1:n.1680-5949T>C
|
|
NM_004518.4:c.2387T>C
|
NP_004509.2:p.Val796Ala
|
|
NM_172106.1:c.2417T>C
|
NP_742104.1:p.Val806Ala
|
|
NM_172107.2:c.2471T>C
|
NP_742105.1:p.Val824Ala
|
|
NM_172108.3:c.2378T>C
|
NP_742106.1:p.Val793Ala
|
|
XM_006723787.1:c.2513T>C
|
XP_006723850.1:p.Val838Ala
|
|
XM_011528807.1:c.2579T>C
|
XP_011527109.1:p.Val860Ala
|
|
XM_011528808.1:c.2576T>C
|
XP_011527110.1:p.Val859Ala
|
|
XM_011528809.1:c.2549T>C
|
XP_011527111.1:p.Val850Ala
|
|
XM_011528810.1:c.2525T>C
|
XP_011527112.1:p.Val842Ala
|
|
XM_011528811.1:c.2495T>C
|
XP_011527113.1:p.Val832Ala
|
|
XM_011528812.1:c.2468T>C
|
XP_011527114.1:p.Val823Ala
|
|
XM_011528813.1:c.2453T>C
|
XP_011527115.1:p.Val818Ala
|
|
XM_011528814.1:c.2060T>C
|
XP_011527116.1:p.Val687Ala
|
|
NM_004518.5:c.2387T>C
|
NP_004509.2:p.Val796Ala
|
|
NM_172106.2:c.2417T>C
|
NP_742104.1:p.Val806Ala
|
|
NM_172107.3:c.2471T>C
|
NP_742105.1:p.Val824Ala
|
|
NM_172108.4:c.2378T>C
|
NP_742106.1:p.Val793Ala
|
|
XM_011528810.2:c.2525T>C
|
XP_011527112.1:p.Val842Ala
|
|
XM_011528811.2:c.2495T>C
|
XP_011527113.1:p.Val832Ala
|
|
XM_017027841.2:c.2522T>C
|
XP_016883330.1:p.Val841Ala
|
|
XM_017027842.2:c.2459T>C
|
XP_016883331.1:p.Val820Ala
|
|
XM_017027843.1:c.2456T>C
|
XP_016883332.1:p.Val819Ala
|
|
XM_017027844.2:c.2414T>C
|
XP_016883333.1:p.Val805Ala
|
|
XM_017027845.1:c.1487T>C
|
XP_016883334.1:p.Val496Ala
|
|
NM_004518.6:c.2387T>C
|
NP_004509.2:p.Val796Ala
|
|
NM_172106.3:c.2417T>C
|
NP_742104.1:p.Val806Ala
|
|
NM_172107.4:c.2471T>C
MANE Select
|
NP_742105.1:p.Val824Ala
|
|
NM_172108.5:c.2378T>C
|
NP_742106.1:p.Val793Ala
|
|
NM_001382235.1:c.2525T>C
|
NP_001369164.1:p.Val842Ala
|
|